HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55154067G>C , CM000681.2:g.55154067G>C | GRCh38 |
NC_000019.9:g.55665435G>C , CM000681.1:g.55665435G>C | GRCh37 |
NC_000019.8:g.60357247G>C | NCBI36 |
NG_007866.2:g.8666C>G , LRG_432:g.8666C>G | |
NG_011829.2:g.172C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344887.10:c.512C>G MANE Select | ENSP00000341838.5:p.Ala171Gly | |
ENST00000665070.1:c.545C>G | ENSP00000499482.1:p.Ala182Gly | |
ENST00000344887.9:c.512C>G | ENSP00000341838.5:p.Ala171Gly | |
ENST00000585806.5:n.511C>G | ||
ENST00000588882.1:c.437C>G | ENSP00000466729.1:p.Ala146Gly | |
ENST00000589864.1:n.340C>G | ||
NM_000363.4:c.512C>G , LRG_432t1:c.512C>G | NP_000354.4:p.Ala171Gly | |
NM_000363.5:c.512C>G MANE Select | NP_000354.4:p.Ala171Gly |