Linked Data
gnomAD v4:
10-102837488-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102837488C>T , CM000672.2:g.102837488C>T | GRCh38 |
| NC_000010.10:g.104597245C>T , CM000672.1:g.104597245C>T | GRCh37 |
| NC_000010.9:g.104587235C>T | NCBI36 |
| NG_007955.1:g.5046G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369887.3:c.-127G>A | ENSP00000358903.3:n.-127G>A | |
| NM_000102.3:c.-127G>A | NP_000093.1:n.-127G>A |