Linked Data
gnomAD v4:
2-38076292-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38076292G>T , CM000664.2:g.38076292G>T | GRCh38 |
| NC_000002.11:g.38303434G>T , CM000664.1:g.38303434G>T | GRCh37 |
| NC_000002.10:g.38156938G>T | NCBI36 |
| NG_008386.2:g.4810C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000494864.1:c.-70-4982C>A | ENSP00000479876.1:n.-70-4982C>A | |
| XM_011533236.1:c.906G>T | XP_011531538.1:p.Arg302= |