Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.135028828C>A , CM000667.2:g.135028828C>A | GRCh38 |
| NC_000005.9:g.134364518C>A , CM000667.1:g.134364518C>A | GRCh37 |
| NC_000005.8:g.134392417C>A | NCBI36 |
| NG_012114.1:g.10447G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000265340.12:c.896G>T MANE Select | ENSP00000265340.6:p.Gly299Val | |
| ENST00000265340.11:c.896G>T | ENSP00000265340.6:p.Gly299Val | |
| ENST00000506438.5:c.896G>T | ENSP00000427542.1:p.Gly299Val | |
| NM_002653.4:c.896G>T | NP_002644.4:p.Gly299Val | |
| NM_002653.5:c.896G>T MANE Select | NP_002644.4:p.Gly299Val |