Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218165120A= , CM000664.2:g.218165120A= | GRCh38 |
| NC_000002.11:g.219029843A= , CM000664.1:g.219029843A= | GRCh37 |
| NC_000002.10:g.218738088A= | NCBI36 |
| NG_011814.1:g.6874T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000634.3:c.92T= MANE Select | NP_000625.1:p.Met31= |
| ENST00000295683.3:c.92T= MANE Select | ENSP00000295683.2:p.Met31= |
| NM_000634.2:c.92T= | NP_000625.1:p.Met31= |
| ENST00000295683.2:c.92T= | ENSP00000295683.2:p.Met31= |