Linked Data
ClinVar Variation Id:
2869390
ClinVar RCV Id:
RCV003705531
gnomAD v4:
2-43948161-A-G
MyVariant Identifiers:
chr2:g.44175300A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43948161A>G , CM000664.2:g.43948161A>G | GRCh38 |
| NC_000002.11:g.44175300A>G , CM000664.1:g.44175300A>G | GRCh37 |
| NC_000002.10:g.44028804A>G | NCBI36 |
| NG_008247.1:g.52845T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409659.6:c.1881T>C | ENSP00000386562.2:p.Arg627= | |
| ENST00000447246.2:c.1881T>C | ENSP00000403637.2:p.Arg627= | |
| ENST00000467058.2:n.610T>C | ||
| ENST00000681959.1:n.1495T>C | ||
| ENST00000681961.1:n.1901T>C | ||
| ENST00000682104.1:c.1755T>C | ENSP00000507716.1:p.Arg585= | |
| ENST00000682303.1:c.*1753T>C | ENSP00000508325.1:n.*1753T>C | |
| ENST00000682308.1:c.1881T>C | ENSP00000507056.1:p.Arg627= | |
| ENST00000682480.1:c.1881T>C | ENSP00000508344.1:p.Arg627= | |
| ENST00000682546.1:c.1878T>C | ENSP00000508188.1:p.Arg626= | |
| ENST00000682585.1:c.1881T>C | ENSP00000506885.1:p.Arg627= | |
| ENST00000682595.1:n.2463T>C | ||
| ENST00000682607.1:c.299T>C | ||
| ENST00000682779.1:c.1872T>C | ENSP00000507947.1:p.Arg624= | |
| ENST00000682885.1:c.1881T>C | ENSP00000508036.1:p.Arg627= | |
| ENST00000682933.1:n.1955T>C | ||
| ENST00000683072.1:n.2463T>C | ||
| ENST00000683082.1:n.1899T>C | ||
| ENST00000683125.1:c.1881T>C | ENSP00000507939.1:p.Arg627= | |
| ENST00000683213.1:c.1884T>C | ENSP00000507751.1:p.Arg628= | |
| ENST00000683220.1:c.1911T>C | ENSP00000507151.1:p.Arg637= | |
| ENST00000683329.1:n.2684T>C | ||
| ENST00000683346.1:c.*1756T>C | ENSP00000507458.1:n.*1756T>C | |
| ENST00000683459.1:n.2468T>C | ||
| ENST00000683590.1:c.1881T>C | ENSP00000506820.1:p.Arg627= | |
| ENST00000683623.1:c.1881T>C | ENSP00000507702.1:p.Arg627= | |
| ENST00000683645.1:n.2432T>C | ||
| ENST00000683694.1:n.632T>C | ||
| ENST00000683796.1:c.*1753T>C | ENSP00000508221.1:n.*1753T>C | |
| ENST00000683802.1:n.4806T>C | ||
| ENST00000683833.1:c.1872T>C | ENSP00000506852.1:p.Arg624= | |
| ENST00000683934.1:c.1767T>C | ||
| ENST00000683989.1:c.1881T>C | ENSP00000507510.1:p.Arg627= | |
| ENST00000683994.1:c.1881T>C | ENSP00000507181.1:p.Arg627= | |
| ENST00000684290.1:c.1881T>C | ENSP00000507243.1:p.Arg627= | |
| ENST00000684306.1:c.*1794T>C | ENSP00000508384.1:n.*1794T>C | |
| ENST00000684341.1:n.1901T>C | ||
| ENST00000684383.1:c.*1519T>C | ENSP00000506863.1:n.*1519T>C | |
| ENST00000684482.1:c.4350T>C | ||
| ENST00000684619.1:c.*1753T>C | ENSP00000508088.1:n.*1753T>C | |
| ENST00000684743.1:n.2912T>C | ||
| ENST00000260665.12:c.1881T>C MANE Select | ENSP00000260665.7:p.Arg627= | |
| ENST00000260665.11:c.1881T>C | ENSP00000260665.7:p.Arg627= | |
| NM_133259.3:c.1881T>C | NP_573566.2:p.Arg627= | |
| XM_006711915.2:c.1803T>C | XP_006711978.1:p.Arg601= | |
| XM_006711916.2:c.1881T>C | XP_006711979.1:p.Arg627= | |
| XM_011532473.1:c.1881T>C | XP_011530775.1:p.Arg627= | |
| XM_011532474.1:c.1881T>C | XP_011530776.1:p.Arg627= | |
| XM_006711916.3:c.1881T>C | XP_006711979.1:p.Arg627= | |
| XM_017003117.1:c.1803T>C | XP_016858606.1:p.Arg601= | |
| XR_002958896.1:n.1923T>C | ||
| NM_133259.4:c.1881T>C MANE Select | NP_573566.2:p.Arg627= |