Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21744538A>T , CM000669.2:g.21744538A>T | GRCh38 |
| NC_000007.13:g.21784156A>T , CM000669.1:g.21784156A>T | GRCh37 |
| NC_000007.12:g.21750681A>T | NCBI36 |
| NG_012886.2:g.206324A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.8255A>T MANE Select | NP_001264044.1:p.Asp2752Val |
| ENST00000409508.8:c.8255A>T MANE Select | ENSP00000475939.1:p.Asp2752Val |
| NM_001277115.1:c.8255A>T | NP_001264044.1:p.Asp2752Val |
| ENST00000328843.10:c.8276A>T | ENSP00000330671.7:p.Asp2759Val |
| ENST00000409508.7:c.8255A>T | ENSP00000475939.1:p.Asp2752Val |
| ENST00000605912.1:c.475-332A>T | ENSP00000476068.1:n.475-332A>T |
| ENST00000620169.4:c.8276A>T | ENSP00000481693.1:p.Asp2759Val |