HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20192682C= , CM000675.2:g.20192682C= | GRCh38 |
NC_000013.10:g.20766821C= , CM000675.1:g.20766821C= | GRCh37 |
NC_000013.9:g.19664821C= | NCBI36 |
NG_008358.1:g.5294G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382848.5:c.-23+101G= MANE Select | ENSP00000372299.4:n.-23+101G= | |
ENST00000382848.4:c.-23+101G= | ENSP00000372299.4:n.-23+101G= | |
NM_004004.5:c.-23+101G= | NP_003995.2:n.-23+101G= | |
NM_004004.6:c.-23+101G= MANE Select | NP_003995.2:n.-23+101G= |