Linked Data
dbSNP Id:
rs370126306
ExAC:
13:110831574 C / T
gnomAD v2:
13-110831574-C-T
gnomAD v3:
13-110179227-C-T
gnomAD v4:
13-110179227-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110179227C>T , CM000675.2:g.110179227C>T | GRCh38 |
| NC_000013.10:g.110831574C>T , CM000675.1:g.110831574C>T | GRCh37 |
| NC_000013.9:g.109629575C>T | NCBI36 |
| NG_011544.2:g.132923G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375820.10:c.2344+44G>A MANE Select | ENSP00000364979.4:n.2344+44G>A | |
| ENST00000649738.1:n.2474+44G>A | ||
| ENST00000375820.8:c.2344+44G>A | ENSP00000364979.4:n.2344+44G>A | |
| NM_001845.5:c.2344+44G>A | NP_001836.3:n.2344+44G>A | |
| XM_011521048.1:c.2152+44G>A | XP_011519350.1:n.2152+44G>A | |
| XM_011521048.2:c.2152+44G>A | XP_011519350.1:n.2152+44G>A | |
| NM_001845.6:c.2344+44G>A MANE Select | NP_001836.3:n.2344+44G>A |