Linked Data
ClinVar Variation Id:
1898274
ClinVar RCV Id:
RCV002579800
dbSNP Id:
rs185834040
ExAC:
9:3932341 G / A
gnomAD v2:
9-3932341-G-A
gnomAD v3:
9-3932341-G-A
gnomAD v4:
9-3932341-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.3932341G>A , CM000671.2:g.3932341G>A | GRCh38 |
| NC_000009.11:g.3932341G>A , CM000671.1:g.3932341G>A | GRCh37 |
| NC_000009.10:g.3922341G>A | NCBI36 |
| NG_011782.1:g.372695C>T | |
| NG_011782.2:g.372695C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463680.6:n.273+19C>T | ||
| ENST00000464391.2:n.541+19C>T | ||
| ENST00000491889.6:c.*1346+19C>T | ENSP00000419914.1:n.*1346+19C>T | |
| ENST00000645252.2:n.425+19C>T | ||
| ENST00000682749.1:c.1518+19C>T | ENSP00000507306.1:n.1518+19C>T | |
| ENST00000682846.1:c.132-102849C>T | ENSP00000507527.1:n.132-102849C>T | |
| ENST00000682864.1:n.482+19C>T | ||
| ENST00000381971.8:c.1983+19C>T MANE Select | ENSP00000371398.3:n.1983+19C>T | |
| ENST00000645252.1:n.425+19C>T | ||
| ENST00000324333.14:c.1518+19C>T | ENSP00000325494.10:n.1518+19C>T | |
| ENST00000381971.7:c.1983+19C>T | ENSP00000371398.3:n.1983+19C>T | |
| ENST00000461870.5:n.339+19C>T | ||
| ENST00000463680.5:n.273+19C>T | ||
| ENST00000467497.6:n.523+19C>T | ||
| NM_001042413.1:c.1983+19C>T | NP_001035878.1:n.1983+19C>T | |
| NM_152629.3:c.1518+19C>T | NP_689842.3:n.1518+19C>T | |
| XM_005251386.3:c.1518+19C>T | XP_005251443.1:n.1518+19C>T | |
| XM_005251387.3:c.1317+19C>T | XP_005251444.1:n.1317+19C>T | |
| XM_005251388.3:c.1317+19C>T | XP_005251445.1:n.1317+19C>T | |
| XM_011517763.1:c.1983+19C>T | XP_011516065.1:n.1983+19C>T | |
| XM_011517764.1:c.1983+19C>T | XP_011516066.1:n.1983+19C>T | |
| XM_011517765.1:c.1983+19C>T | XP_011516067.1:n.1983+19C>T | |
| XM_011517766.1:c.1518+19C>T | XP_011516068.1:n.1518+19C>T | |
| XM_011517767.1:c.1317+19C>T | XP_011516069.1:n.1317+19C>T | |
| XM_005251386.4:c.1518+19C>T | XP_005251443.1:n.1518+19C>T | |
| XM_005251387.4:c.1317+19C>T | XP_005251444.1:n.1317+19C>T | |
| XM_005251388.4:c.1317+19C>T | XP_005251445.1:n.1317+19C>T | |
| XM_011517763.2:c.1983+19C>T | XP_011516065.1:n.1983+19C>T | |
| XM_011517764.2:c.1983+19C>T | XP_011516066.1:n.1983+19C>T | |
| XM_011517765.2:c.1983+19C>T | XP_011516067.1:n.1983+19C>T | |
| XM_011517766.2:c.1518+19C>T | XP_011516068.1:n.1518+19C>T | |
| XM_011517767.3:c.1317+19C>T | XP_011516069.1:n.1317+19C>T | |
| XM_017014361.1:c.1518+19C>T | XP_016869850.1:n.1518+19C>T | |
| NM_001042413.2:c.1983+19C>T MANE Select | NP_001035878.1:n.1983+19C>T | |
| NM_152629.4:c.1518+19C>T | NP_689842.3:n.1518+19C>T |