Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21867961C>T , CM000669.2:g.21867961C>T | GRCh38 |
| NC_000007.13:g.21907579C>T , CM000669.1:g.21907579C>T | GRCh37 |
| NC_000007.12:g.21874104C>T | NCBI36 |
| NG_012886.2:g.329747C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001277115.2:c.11793C>T MANE Select | NP_001264044.1:p.Phe3931= |
| ENST00000409508.8:c.11793C>T MANE Select | ENSP00000475939.1:p.Phe3931= |
| NM_001277115.1:c.11793C>T | NP_001264044.1:p.Phe3931= |
| ENST00000328843.10:c.11814C>T | ENSP00000330671.7:p.Phe3938= |
| ENST00000409508.7:c.11793C>T | ENSP00000475939.1:p.Phe3931= |
| ENST00000620169.4:c.11814C>T | ENSP00000481693.1:p.Phe3938= |