Linked Data
gnomAD v4:
10-102837490-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.102837490T>C , CM000672.2:g.102837490T>C | GRCh38 |
| NC_000010.10:g.104597247T>C , CM000672.1:g.104597247T>C | GRCh37 |
| NC_000010.9:g.104587237T>C | NCBI36 |
| NG_007955.1:g.5044A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369887.3:c.-129A>G | ENSP00000358903.3:n.-129A>G | |
| NM_000102.3:c.-129A>G | NP_000093.1:n.-129A>G |