Linked Data
dbSNP Id:
rs376410059
ExAC:
4:40356314 G / C
gnomAD v3:
4-40354297-G-C
gnomAD v4:
4-40354297-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.40354297G>C , CM000666.2:g.40354297G>C | GRCh38 |
| NC_000004.11:g.40356314G>C , CM000666.1:g.40356314G>C | GRCh37 |
| NC_000004.10:g.40051071G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310169.3:c.1217G>C MANE Select | ENSP00000312663.2:p.Cys406Ser | |
| ENST00000310169.2:c.1217G>C | ENSP00000312663.2:p.Cys406Ser | |
| NM_017581.3:c.1217G>C | NP_060051.2:p.Cys406Ser | |
| NM_017581.4:c.1217G>C MANE Select | NP_060051.2:p.Cys406Ser |