HGVS | Genome Assembly |
---|---|
NC_000010.11:g.100045666T>C , CM000672.2:g.100045666T>C | GRCh38 |
NC_000010.10:g.101805423T>C , CM000672.1:g.101805423T>C | GRCh37 |
NC_000010.9:g.101795413T>C | NCBI36 |
NG_012060.1:g.41220A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370418.8:c.1231-3093A>G MANE Select | ENSP00000359446.3:n.1231-3093A>G | |
ENST00000370418.7:c.1231-3093A>G | ENSP00000359446.3:n.1231-3093A>G | |
NM_001308.2:c.1231-3093A>G | NP_001299.1:n.1231-3093A>G | |
XM_011539299.1:c.1273-3093A>G | XP_011537601.1:n.1273-3093A>G | |
NM_001308.3:c.1231-3093A>G MANE Select | NP_001299.1:n.1231-3093A>G |