Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.240872967C= , CM000664.2:g.240872967C= | GRCh38 |
| NC_000002.11:g.241812384C= , CM000664.1:g.241812384C= | GRCh37 |
| NC_000002.10:g.241461057C= | NCBI36 |
| NG_008005.1:g.9223C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307503.4:c.525-12C= MANE Select | ENSP00000302620.3:n.525-12C= | |
| ENST00000307503.3:c.525-12C= | ENSP00000302620.3:n.525-12C= | |
| ENST00000472436.1:n.545-12C= | ||
| ENST00000476698.1:n.262-12C= | ||
| NM_000030.2:c.525-12C= | NP_000021.1:n.525-12C= | |
| NM_000030.3:c.525-12C= MANE Select | NP_000021.1:n.525-12C= |