Linked Data
dbSNP Id:
rs748765329
ExAC:
11:1861776 G / C
gnomAD v2:
11-1861776-G-C
gnomAD v4:
11-1840546-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.1840546G>C , CM000673.2:g.1840546G>C | GRCh38 |
| NC_000011.9:g.1861776G>C , CM000673.1:g.1861776G>C | GRCh37 |
| NC_000011.8:g.1818352G>C | NCBI36 |
| NG_011621.1:g.6544G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381911.6:c.76G>C MANE Select | ENSP00000371336.1:p.Ala26Pro | |
| ENST00000252898.11:c.76G>C | ENSP00000252898.7:p.Ala26Pro | |
| ENST00000381905.3:c.76G>C | ENSP00000371330.3:p.Ala26Pro | |
| ENST00000381906.5:c.76G>C | ENSP00000371331.1:p.Ala26Pro | |
| ENST00000381911.5:c.76G>C | ENSP00000371336.1:p.Ala26Pro | |
| ENST00000468473.1:n.246G>C | ||
| ENST00000617947.4:c.76G>C | ENSP00000481242.1:p.Ala26Pro | |
| NM_001145829.1:c.76G>C | NP_001139301.1:p.Ala26Pro | |
| NM_001145841.1:c.76G>C | NP_001139313.1:p.Ala26Pro | |
| NM_003282.3:c.76G>C | NP_003273.1:p.Ala26Pro | |
| NM_003282.4:c.76G>C MANE Select | NP_003273.1:p.Ala26Pro | |
| NM_001145829.2:c.76G>C | NP_001139301.1:p.Ala26Pro | |
| NM_001145841.2:c.76G>C | NP_001139313.1:p.Ala26Pro |