Linked Data
gnomAD v4:
8-38144221-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38144221T>G , CM000670.2:g.38144221T>G | GRCh38 |
| NC_000008.10:g.38001739T>G , CM000670.1:g.38001739T>G | GRCh37 |
| NC_000008.9:g.38120896T>G | NCBI36 |
| NG_011827.1:g.11862A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.*52A>C MANE Select | ENSP00000276449.3:n.*52A>C | |
| ENST00000276449.8:c.*52A>C | ENSP00000276449.3:n.*52A>C | |
| ENST00000520114.1:n.2879A>C | ||
| NM_000349.2:c.*52A>C | NP_000340.2:n.*52A>C | |
| XM_006716392.1:c.816A>C | XP_006716455.1:p.Ser272= | |
| NM_000349.3:c.*52A>C MANE Select | NP_000340.2:n.*52A>C |