HGVS | Genome Assembly |
---|---|
NC_000013.11:g.107427835T>G , CM000675.2:g.107427835T>G | GRCh38 |
NC_000013.10:g.108080183T>G , CM000675.1:g.108080183T>G | GRCh37 |
NC_000013.9:g.106878184T>G | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000375915.4:c.916-217080A>C MANE Select | ENSP00000365080.1:n.916-217080A>C | |
ENST00000375915.3:c.916-217080A>C | ENSP00000365080.1:n.916-217080A>C | |
NM_001080396.2:c.916-217080A>C | NP_001073865.1:n.916-217080A>C | |
XM_011521109.1:c.916-217080A>C | XP_011519411.1:n.916-217080A>C | |
XM_011521109.3:c.916-217080A>C | XP_011519411.1:n.916-217080A>C | |
NM_001080396.3:c.916-217080A>C MANE Select | NP_001073865.1:n.916-217080A>C |