Linked Data
gnomAD v4:
4-24800162-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800162G>C , CM000666.2:g.24800162G>C | GRCh38 |
| NC_000004.11:g.24801784G>C , CM000666.1:g.24801784G>C | GRCh37 |
| NC_000004.10:g.24410882G>C | NCBI36 |
| NG_012213.1:g.9700G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.641G>C MANE Select | ENSP00000371554.3:p.Gly214Ala | |
| ENST00000382120.3:c.641G>C | ENSP00000371554.3:p.Gly214Ala | |
| NM_003102.2:c.641G>C | NP_003093.2:p.Gly214Ala | |
| XR_427488.1:n.831G>C | ||
| NM_003102.3:c.641G>C | NP_003093.2:p.Gly214Ala | |
| NM_003102.4:c.641G>C MANE Select | NP_003093.2:p.Gly214Ala |