Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112226508C>G , CM000673.2:g.112226508C>G | GRCh38 |
| NC_000011.9:g.112097231C>G , CM000673.1:g.112097231C>G | GRCh37 |
| NC_000011.8:g.111602441C>G | NCBI36 |
| NG_008743.1:g.5144C>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000317.3:c.65C>G MANE Select | NP_000308.1:p.Ala22Gly |
| ENST00000280362.8:c.65C>G MANE Select | ENSP00000280362.3:p.Ala22Gly |
| NM_000317.2:c.65C>G | NP_000308.1:p.Ala22Gly |
| ENST00000280362.7:c.65C>G | ENSP00000280362.3:p.Ala22Gly |
| ENST00000525645.1:n.140C>G | |
| ENST00000525803.1:c.65C>G | ENSP00000431750.1:p.Ala22Gly |
| ENST00000528679.5:c.65C>G | ENSP00000435895.1:p.Ala22Gly |
| ENST00000531673.5:c.65C>G | ENSP00000433469.1:p.Ala22Gly |