Linked Data
gnomAD v4:
10-102837439-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102837439T>A , CM000672.2:g.102837439T>A | GRCh38 |
| NC_000010.10:g.104597196T>A , CM000672.1:g.104597196T>A | GRCh37 |
| NC_000010.9:g.104587186T>A | NCBI36 |
| NG_007955.1:g.5095A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000638190.1:c.-78A>T | ENSP00000492539.1:n.-78A>T | |
| ENST00000638971.1:c.-78A>T | ENSP00000492313.1:n.-78A>T | |
| ENST00000369887.3:c.-78A>T | ENSP00000358903.3:n.-78A>T | |
| NM_000102.3:c.-78A>T | NP_000093.1:n.-78A>T |