Linked Data
dbSNP Id:
rs782159498
ExAC:
X:154250638 T / A
gnomAD v2:
X-154250638-T-A
gnomAD v4:
X-155022363-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155022363T>A , CM000685.2:g.155022363T>A | GRCh38 |
| NC_000023.10:g.154250638T>A , CM000685.1:g.154250638T>A | GRCh37 |
| NC_000023.9:g.153903832T>A | NCBI36 |
| NG_011403.1:g.5361A>T | |
| NG_011403.2:g.5361A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000360256.9:c.143+47A>T MANE Select | ENSP00000353393.4:n.143+47A>T | |
| ENST00000647125.1:c.121+69A>T | ENSP00000496062.1:n.121+69A>T | |
| ENST00000360256.8:c.143+47A>T | ENSP00000353393.4:n.143+47A>T | |
| ENST00000423959.5:c.38+4417A>T | ENSP00000409446.1:n.38+4417A>T | |
| ENST00000453950.1:c.125+47A>T | ENSP00000389153.1:n.125+47A>T | |
| NM_000132.3:c.143+47A>T | NP_000123.1:n.143+47A>T | |
| XM_011531126.1:c.38+4417A>T | XP_011529428.1:n.38+4417A>T | |
| NM_000132.4:c.143+47A>T MANE Select | NP_000123.1:n.143+47A>T |