Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240869051G= , CM000664.2:g.240869051G= | GRCh38 |
| NC_000002.11:g.241808468G= , CM000664.1:g.241808468G= | GRCh37 |
| NC_000002.10:g.241457141G= | NCBI36 |
| NG_008005.1:g.5307G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.165+21G= MANE Select | ENSP00000302620.3:n.165+21G= | |
| ENST00000307503.3:c.165+21G= | ENSP00000302620.3:n.165+21G= | |
| ENST00000472436.1:n.185+21G= | ||
| NM_000030.2:c.165+21G= | NP_000021.1:n.165+21G= | |
| XR_924060.1:n.405+1182C= | ||
| NM_000030.3:c.165+21G= MANE Select | NP_000021.1:n.165+21G= |