HGVS | Genome Assembly |
---|---|
NC_000005.10:g.41475664C>T , CM000667.2:g.41475664C>T | GRCh38 |
NC_000005.9:g.41475766C>T , CM000667.1:g.41475766C>T | GRCh37 |
NC_000005.8:g.41511523C>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000377801.8:c.103+34760G>A MANE Select | ENSP00000367032.3:n.103+34760G>A | |
ENST00000328457.5:c.103+34760G>A | ENSP00000333751.3:n.103+34760G>A | |
ENST00000377801.7:c.103+34760G>A | ENSP00000367032.3:n.103+34760G>A | |
NM_001005473.2:c.103+34760G>A | NP_001005473.1:n.103+34760G>A | |
NM_001005473.3:c.103+34760G>A MANE Select | NP_001005473.1:n.103+34760G>A |