Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35509260C>T , CM000668.2:g.35509260C>T | GRCh38 |
| NC_000006.11:g.35477037C>T , CM000668.1:g.35477037C>T | GRCh37 |
| NC_000006.10:g.35585015C>T | NCBI36 |
| NG_009077.1:g.8611G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003322.6:c.771G>A MANE Select | NP_003313.3:p.Thr257= |
| ENST00000229771.11:c.771G>A MANE Select | ENSP00000229771.6:p.Thr257= |
| NM_001289395.1:c.612G>A | NP_001276324.1:p.Thr204= |
| NM_001289395.2:c.612G>A | NP_001276324.1:p.Thr204= |
| NM_003322.4:c.771G>A | NP_003313.3:p.Thr257= |
| NM_003322.5:c.771G>A | NP_003313.3:p.Thr257= |
| ENST00000229771.10:c.771G>A | ENSP00000229771.6:p.Thr257= |
| ENST00000322263.8:c.612G>A | ENSP00000319414.4:p.Thr204= |
| ENST00000373892.4:n.373G>A | |
| ENST00000614066.4:c.771G>A | ENSP00000477534.1:p.Thr257= |