Linked Data
dbSNP Id:
rs754515623
ExAC:
11:1861777 C / T
gnomAD v2:
11-1861777-C-T
gnomAD v3:
11-1840547-C-T
gnomAD v4:
11-1840547-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1840547C>T , CM000673.2:g.1840547C>T | GRCh38 |
| NC_000011.9:g.1861777C>T , CM000673.1:g.1861777C>T | GRCh37 |
| NC_000011.8:g.1818353C>T | NCBI36 |
| NG_011621.1:g.6545C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381911.6:c.77C>T MANE Select | ENSP00000371336.1:p.Ala26Val | |
| ENST00000252898.11:c.77C>T | ENSP00000252898.7:p.Ala26Val | |
| ENST00000381905.3:c.77C>T | ENSP00000371330.3:p.Ala26Val | |
| ENST00000381906.5:c.77C>T | ENSP00000371331.1:p.Ala26Val | |
| ENST00000381911.5:c.77C>T | ENSP00000371336.1:p.Ala26Val | |
| ENST00000468473.1:n.247C>T | ||
| ENST00000617947.4:c.77C>T | ENSP00000481242.1:p.Ala26Val | |
| NM_001145829.1:c.77C>T | NP_001139301.1:p.Ala26Val | |
| NM_001145841.1:c.77C>T | NP_001139313.1:p.Ala26Val | |
| NM_003282.3:c.77C>T | NP_003273.1:p.Ala26Val | |
| NM_003282.4:c.77C>T MANE Select | NP_003273.1:p.Ala26Val | |
| NM_001145829.2:c.77C>T | NP_001139301.1:p.Ala26Val | |
| NM_001145841.2:c.77C>T | NP_001139313.1:p.Ala26Val |