HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23222704T>C , CM000670.2:g.23222704T>C | GRCh38 |
NC_000008.10:g.23080217T>C , CM000670.1:g.23080217T>C | GRCh37 |
NC_000008.9:g.23136162T>C | NCBI36 |
NG_032107.1:g.7464A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221132.8:c.306+2052A>G MANE Select | ENSP00000221132.3:n.306+2052A>G | |
ENST00000221132.7:c.306+2052A>G | ENSP00000221132.3:n.306+2052A>G | |
ENST00000524158.5:c.-301+1729A>G | ENSP00000428884.1:n.-301+1729A>G | |
ENST00000613472.1:c.31+2327A>G | ENSP00000480778.1:n.31+2327A>G | |
NM_003844.3:c.306+2052A>G | NP_003835.3:n.306+2052A>G | |
NM_003844.4:c.306+2052A>G MANE Select | NP_003835.3:n.306+2052A>G |