Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96301050T>C , CM000664.2:g.96301050T>C | GRCh38 |
| NC_000002.11:g.96966788T>C , CM000664.1:g.96966788T>C | GRCh37 |
| NC_000002.10:g.96330515T>C | NCBI36 |
| NG_016973.1:g.9510A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014014.5:c.578A>G MANE Select | NP_054733.2:p.Asp193Gly |
| ENST00000323853.10:c.578A>G MANE Select | ENSP00000317123.5:p.Asp193Gly |
| NM_014014.4:c.578A>G | NP_054733.2:p.Asp193Gly |
| ENST00000323853.9:c.578A>G | ENSP00000317123.5:p.Asp193Gly |
| ENST00000652267.1:c.578A>G | ENSP00000498933.1:p.Asp193Gly |