Linked Data
ClinVar Variation Id:
336160
dbSNP Id:
rs374995996
ExAC:
2:44177705 G / A
gnomAD v2:
2-44177705-G-A
gnomAD v3:
2-43950566-G-A
gnomAD v4:
2-43950566-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43950566G>A , CM000664.2:g.43950566G>A | GRCh38 |
| NC_000002.11:g.44177705G>A , CM000664.1:g.44177705G>A | GRCh37 |
| NC_000002.10:g.44031209G>A | NCBI36 |
| NG_008247.1:g.50440C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409659.6:c.1677+7C>T | ENSP00000386562.2:n.1677+7C>T | |
| ENST00000447246.2:c.1677+7C>T | ENSP00000403637.2:n.1677+7C>T | |
| ENST00000467058.2:n.406+7C>T | ||
| ENST00000681959.1:n.1291+7C>T | ||
| ENST00000681961.1:n.1697+7C>T | ||
| ENST00000682104.1:c.1551+7C>T | ENSP00000507716.1:n.1551+7C>T | |
| ENST00000682303.1:c.*1549+7C>T | ENSP00000508325.1:n.*1549+7C>T | |
| ENST00000682308.1:c.1677+7C>T | ENSP00000507056.1:n.1677+7C>T | |
| ENST00000682480.1:c.1677+7C>T | ENSP00000508344.1:n.1677+7C>T | |
| ENST00000682546.1:c.1677+7C>T | ENSP00000508188.1:n.1677+7C>T | |
| ENST00000682585.1:c.1677+7C>T | ENSP00000506885.1:n.1677+7C>T | |
| ENST00000682595.1:n.2259+7C>T | ||
| ENST00000682607.1:c.95+7C>T | ||
| ENST00000682779.1:c.1668+7C>T | ENSP00000507947.1:n.1668+7C>T | |
| ENST00000682885.1:c.1677+7C>T | ENSP00000508036.1:n.1677+7C>T | |
| ENST00000682933.1:n.1751+7C>T | ||
| ENST00000683072.1:n.2259+7C>T | ||
| ENST00000683082.1:n.1695+7C>T | ||
| ENST00000683125.1:c.1677+7C>T | ENSP00000507939.1:n.1677+7C>T | |
| ENST00000683213.1:c.1680+7C>T | ENSP00000507751.1:n.1680+7C>T | |
| ENST00000683220.1:c.1677+7C>T | ENSP00000507151.1:n.1677+7C>T | |
| ENST00000683329.1:n.2480+7C>T | ||
| ENST00000683346.1:c.*1552+7C>T | ENSP00000507458.1:n.*1552+7C>T | |
| ENST00000683459.1:n.2264+7C>T | ||
| ENST00000683590.1:c.1677+7C>T | ENSP00000506820.1:n.1677+7C>T | |
| ENST00000683623.1:c.1677+7C>T | ENSP00000507702.1:n.1677+7C>T | |
| ENST00000683645.1:n.2197+7C>T | ||
| ENST00000683694.1:n.428+7C>T | ||
| ENST00000683796.1:c.*1549+7C>T | ENSP00000508221.1:n.*1549+7C>T | |
| ENST00000683802.1:n.4602+7C>T | ||
| ENST00000683833.1:c.1668+7C>T | ENSP00000506852.1:n.1668+7C>T | |
| ENST00000683934.1:c.1563+7C>T | ||
| ENST00000683989.1:c.1677+7C>T | ENSP00000507510.1:n.1677+7C>T | |
| ENST00000683994.1:c.1677+7C>T | ENSP00000507181.1:n.1677+7C>T | |
| ENST00000684290.1:c.1677+7C>T | ENSP00000507243.1:n.1677+7C>T | |
| ENST00000684306.1:c.*1590+7C>T | ENSP00000508384.1:n.*1590+7C>T | |
| ENST00000684341.1:n.1697+7C>T | ||
| ENST00000684383.1:c.*1315+7C>T | ENSP00000506863.1:n.*1315+7C>T | |
| ENST00000684482.1:c.4146+7C>T | ||
| ENST00000684619.1:c.*1549+7C>T | ENSP00000508088.1:n.*1549+7C>T | |
| ENST00000684743.1:n.2708+7C>T | ||
| ENST00000260665.12:c.1677+7C>T MANE Select | ENSP00000260665.7:n.1677+7C>T | |
| ENST00000260665.11:c.1677+7C>T | ENSP00000260665.7:n.1677+7C>T | |
| ENST00000467058.1:n.406+7C>T | ||
| NM_133259.3:c.1677+7C>T | NP_573566.2:n.1677+7C>T | |
| XM_006711915.2:c.1599+7C>T | XP_006711978.1:n.1599+7C>T | |
| XM_006711916.2:c.1677+7C>T | XP_006711979.1:n.1677+7C>T | |
| XM_011532473.1:c.1677+7C>T | XP_011530775.1:n.1677+7C>T | |
| XM_011532474.1:c.1677+7C>T | XP_011530776.1:n.1677+7C>T | |
| XM_006711916.3:c.1677+7C>T | XP_006711979.1:n.1677+7C>T | |
| XM_017003117.1:c.1599+7C>T | XP_016858606.1:n.1599+7C>T | |
| XR_002958896.1:n.1719+7C>T | ||
| NM_133259.4:c.1677+7C>T MANE Select | NP_573566.2:n.1677+7C>T |