Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114716124C>T , CM000663.2:g.114716124C>T | GRCh38 |
| NC_000001.10:g.115258745C>T , CM000663.1:g.115258745C>T | GRCh37 |
| NC_000001.9:g.115060268C>T | NCBI36 |
| NG_007572.1:g.5771G>A , LRG_92:g.5771G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002524.5:c.37G>A MANE Select | NP_002515.1:p.Gly13Ser |
| ENST00000369535.5:c.37G>A MANE Select | ENSP00000358548.4:p.Gly13Ser |
| NM_002524.4:c.37G>A | NP_002515.1:p.Gly13Ser |
| ENST00000369535.4:c.37G>A | ENSP00000358548.4:p.Gly13Ser |