Linked Data
ClinVar Variation Id:
368245
dbSNP Id:
rs368357171
ExAC:
X:32398623 T / A
gnomAD v2:
X-32398623-T-A
gnomAD v3:
X-32380506-T-A
gnomAD v4:
X-32380506-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32380506T>A , CM000685.2:g.32380506T>A | GRCh38 |
| NC_000023.10:g.32398623T>A , CM000685.1:g.32398623T>A | GRCh37 |
| NC_000023.9:g.32308544T>A | NCBI36 |
| NG_012232.1:g.964104A>T , LRG_199:g.964104A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357033.9:c.4845+4A>T MANE Select | ENSP00000354923.3:n.4845+4A>T | |
| ENST00000619831.5:c.813+4A>T | ENSP00000479270.2:n.813+4A>T | |
| ENST00000357033.8:c.4845+4A>T | ENSP00000354923.3:n.4845+4A>T | |
| ENST00000378677.6:c.4833+4A>T | ENSP00000367948.2:n.4833+4A>T | |
| ENST00000420596.5:c.94-15307A>T | ENSP00000399897.1:n.94-15307A>T | |
| ENST00000448370.5:c.94-15796A>T | ENSP00000388559.1:n.94-15796A>T | |
| ENST00000488902.5:n.336-163443A>T | ||
| ENST00000619831.4:c.4833+4A>T | ENSP00000479270.1:n.4833+4A>T | |
| ENST00000620040.4:c.4845+4A>T | ENSP00000478150.1:n.4845+4A>T | |
| NM_000109.3:c.4821+4A>T | NP_000100.2:n.4821+4A>T | |
| NM_004006.2:c.4845+4A>T , LRG_199t1:c.4845+4A>T | NP_003997.1:n.4845+4A>T | |
| NM_004009.3:c.4833+4A>T | NP_004000.1:n.4833+4A>T | |
| NM_004010.3:c.4476+4A>T | NP_004001.1:n.4476+4A>T | |
| NM_004011.3:c.822+4A>T | NP_004002.2:n.822+4A>T | |
| NM_004012.3:c.813+4A>T | NP_004003.1:n.813+4A>T | |
| XM_006724468.2:c.4845+4A>T | XP_006724531.1:n.4845+4A>T | |
| XM_006724469.2:c.4821+4A>T | XP_006724532.1:n.4821+4A>T | |
| XM_006724470.2:c.4845+4A>T | XP_006724533.1:n.4845+4A>T | |
| XM_006724471.2:c.4845+4A>T | XP_006724534.1:n.4845+4A>T | |
| XM_006724472.2:c.4716+4A>T | XP_006724535.1:n.4716+4A>T | |
| XM_006724473.2:c.4845+4A>T | XP_006724536.1:n.4845+4A>T | |
| XM_006724474.2:c.4845+4A>T | XP_006724537.1:n.4845+4A>T | |
| XM_006724475.2:c.4845+4A>T | XP_006724538.1:n.4845+4A>T | |
| XM_011545467.1:c.4845+4A>T | XP_011543769.1:n.4845+4A>T | |
| XM_011545468.1:c.4845+4A>T | XP_011543770.1:n.4845+4A>T | |
| XM_011545469.1:c.4845+4A>T | XP_011543771.1:n.4845+4A>T | |
| XM_006724469.3:c.4821+4A>T | XP_006724532.1:n.4821+4A>T | |
| XM_006724470.3:c.4845+4A>T | XP_006724533.1:n.4845+4A>T | |
| XM_006724474.3:c.4845+4A>T | XP_006724537.1:n.4845+4A>T | |
| XM_011545468.2:c.4845+4A>T | XP_011543770.1:n.4845+4A>T | |
| XM_017029328.1:c.4845+4A>T | XP_016884817.1:n.4845+4A>T | |
| XM_017029329.1:c.4845+4A>T | XP_016884818.1:n.4845+4A>T | |
| XM_017029330.2:c.4845+4A>T | XP_016884819.1:n.4845+4A>T | |
| NM_000109.4:c.4821+4A>T | NP_000100.3:n.4821+4A>T | |
| NM_004006.3:c.4845+4A>T MANE Select | NP_003997.2:n.4845+4A>T | |
| NM_004011.4:c.822+4A>T | NP_004002.3:n.822+4A>T | |
| NM_004012.4:c.813+4A>T | NP_004003.2:n.813+4A>T |