HGVS | Genome Assembly |
---|---|
NC_000012.12:g.107059009A>G , CM000674.2:g.107059009A>G | GRCh38 |
NC_000012.11:g.107452787A>G , CM000674.1:g.107452787A>G | GRCh37 |
NC_000012.10:g.105976917A>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000008527.10:c.158+33795T>C MANE Select | ENSP00000008527.5:n.158+33795T>C | |
ENST00000008527.9:c.158+33795T>C | ENSP00000008527.5:n.158+33795T>C | |
NM_004075.4:c.158+33795T>C | NP_004066.1:n.158+33795T>C | |
XM_011537939.1:c.74+13926T>C | XP_011536241.1:n.74+13926T>C | |
XM_017018832.2:c.74+13926T>C | XP_016874321.1:n.74+13926T>C | |
XM_024448844.1:c.158+33795T>C | XP_024304612.1:n.158+33795T>C | |
XM_024448845.1:c.74+13926T>C | XP_024304613.1:n.74+13926T>C | |
NM_004075.5:c.158+33795T>C MANE Select | NP_004066.1:n.158+33795T>C |