HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23222525A= , CM000670.2:g.23222525A= | GRCh38 |
NC_000008.10:g.23080038A= , CM000670.1:g.23080038A= | GRCh37 |
NC_000008.9:g.23135983A= | NCBI36 |
NG_032107.1:g.7643T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000221132.8:c.306+2231T= MANE Select | ENSP00000221132.3:n.306+2231T= | |
ENST00000221132.7:c.306+2231T= | ENSP00000221132.3:n.306+2231T= | |
ENST00000524158.5:c.-301+1908T= | ENSP00000428884.1:n.-301+1908T= | |
ENST00000613472.1:c.31+2506T= | ENSP00000480778.1:n.31+2506T= | |
NM_003844.3:c.306+2231T= | NP_003835.3:n.306+2231T= | |
NM_003844.4:c.306+2231T= MANE Select | NP_003835.3:n.306+2231T= |