Linked Data
gnomAD v4:
11-112086817-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112086817C>T , CM000673.2:g.112086817C>T | GRCh38 |
| NC_000011.9:g.111957541C>T , CM000673.1:g.111957541C>T | GRCh37 |
| NC_000011.8:g.111462751C>T | NCBI36 |
| NG_012337.2:g.4971C>T | |
| NG_033145.1:g.4982G>A | |
| NG_012337.3:g.4971C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375549.7:c.-91C>T | ENSP00000364699.3:n.-91C>T |