Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118110439T>G , CM000670.2:g.118110439T>G | GRCh38 |
| NC_000008.10:g.119122678T>G , CM000670.1:g.119122678T>G | GRCh37 |
| NC_000008.9:g.119191859T>G | NCBI36 |
| NG_007455.2:g.6381A>C , LRG_493:g.6381A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000127.3:c.608A>C MANE Select | NP_000118.2:p.Tyr203Ser |
| ENST00000378204.7:c.608A>C MANE Select | ENSP00000367446.3:p.Tyr203Ser |
| NM_000127.2:c.608A>C , LRG_493t1:c.608A>C | NP_000118.2:p.Tyr203Ser |
| ENST00000378204.6:c.608A>C | ENSP00000367446.2:p.Tyr203Ser |
| ENST00000437196.1:c.73+535A>C | ENSP00000407299.1:n.73+535A>C |