Linked Data
gnomAD v4:
8-38144251-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.38144251G>A , CM000670.2:g.38144251G>A | GRCh38 |
| NC_000008.10:g.38001769G>A , CM000670.1:g.38001769G>A | GRCh37 |
| NC_000008.9:g.38120926G>A | NCBI36 |
| NG_011827.1:g.11832C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000276449.9:c.*22C>T MANE Select | ENSP00000276449.3:n.*22C>T | |
| ENST00000276449.8:c.*22C>T | ENSP00000276449.3:n.*22C>T | |
| ENST00000520114.1:n.2849C>T | ||
| ENST00000522050.1:c.722C>T | ||
| NM_000349.2:c.*22C>T | NP_000340.2:n.*22C>T | |
| XM_006716392.1:c.786C>T | XP_006716455.1:p.Asn262= | |
| NM_000349.3:c.*22C>T MANE Select | NP_000340.2:n.*22C>T |