Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8016229T>G , CM000679.2:g.8016229T>G | GRCh38 |
| NC_000017.10:g.7919547T>G , CM000679.1:g.7919547T>G | GRCh37 |
| NC_000017.9:g.7860272T>G | NCBI36 |
| NG_009092.1:g.18560T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000180.4:c.3163T>G MANE Select | NP_000171.1:p.Trp1055Gly |
| ENST00000254854.5:c.3163T>G MANE Select | ENSP00000254854.4:p.Trp1055Gly |
| NM_000180.3:c.3163T>G | NP_000171.1:p.Trp1055Gly |
| ENST00000254854.4:c.3163T>G | ENSP00000254854.4:p.Trp1055Gly |
| ENST00000574510.1:n.101T>G | |
| XM_011523816.1:c.3163T>G | XP_011522118.1:p.Trp1055Gly |