HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151896A>C , CM000681.2:g.55151896A>C | GRCh38 |
NC_000019.9:g.55663264A>C , CM000681.1:g.55663264A>C | GRCh37 |
NC_000019.8:g.60355076A>C | NCBI36 |
NG_007866.2:g.10837T>G , LRG_432:g.10837T>G | |
NG_011829.2:g.2343T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.571T>G MANE Select | ENSP00000341838.5:p.Trp191Gly | |
ENST00000665070.1:c.604T>G | ENSP00000499482.1:p.Trp202Gly | |
ENST00000344887.9:c.571T>G | ENSP00000341838.5:p.Trp191Gly | |
ENST00000585806.5:n.570T>G | ||
ENST00000588882.1:c.496T>G | ENSP00000466729.1:p.Trp166Gly | |
ENST00000589864.1:n.399T>G | ||
NM_000363.4:c.571T>G , LRG_432t1:c.571T>G | NP_000354.4:p.Trp191Gly | |
NM_000363.5:c.571T>G MANE Select | NP_000354.4:p.Trp191Gly |