HGVS | Genome Assembly |
---|---|
NC_000009.12:g.133352649A>G , CM000671.2:g.133352649A>G | GRCh38 |
NC_000009.10:g.135209325A>G | NCBI36 |
NG_008477.1:g.8858T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371974.8:c.589-41T>C MANE Select | ENSP00000361042.3:n.589-41T>C | |
ENST00000371974.7:c.589-41T>C | ENSP00000361042.3:n.589-41T>C | |
ENST00000437995.1:n.499-41T>C | ||
ENST00000495952.5:n.579-41T>C | ||
ENST00000615505.4:c.262-41T>C | ENSP00000482067.1:n.262-41T>C | |
NM_001280787.1:c.262-41T>C | NP_001267716.1:n.262-41T>C | |
NM_003172.3:c.589-41T>C | NP_003163.1:n.589-41T>C | |
XM_011518942.1:c.262-41T>C | XP_011517244.1:n.262-41T>C | |
NM_003172.4:c.589-41T>C MANE Select | NP_003163.1:n.589-41T>C |