HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23222527A>G , CM000670.2:g.23222527A>G | GRCh38 |
NC_000008.10:g.23080040A>G , CM000670.1:g.23080040A>G | GRCh37 |
NC_000008.9:g.23135985A>G | NCBI36 |
NG_032107.1:g.7641T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221132.8:c.306+2229T>C MANE Select | ENSP00000221132.3:n.306+2229T>C | |
ENST00000221132.7:c.306+2229T>C | ENSP00000221132.3:n.306+2229T>C | |
ENST00000524158.5:c.-301+1906T>C | ENSP00000428884.1:n.-301+1906T>C | |
ENST00000613472.1:c.31+2504T>C | ENSP00000480778.1:n.31+2504T>C | |
NM_003844.3:c.306+2229T>C | NP_003835.3:n.306+2229T>C | |
NM_003844.4:c.306+2229T>C MANE Select | NP_003835.3:n.306+2229T>C |