HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6709797C>T , CM000681.2:g.6709797C>T | GRCh38 |
NC_000019.9:g.6709808C>T , CM000681.1:g.6709808C>T | GRCh37 |
NC_000019.8:g.6660808C>T | NCBI36 |
NG_009557.1:g.15855G>A , LRG_27:g.15855G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.1609G>A | ENSP00000512083.1:p.Gly537Arg | |
ENST00000695654.1:c.856G>A | ENSP00000512085.1:p.Gly286Arg | |
ENST00000695655.1:c.673G>A | ENSP00000512086.1:n.673G>A | |
ENST00000695692.1:n.1096G>A | ||
ENST00000245907.11:c.1732G>A MANE Select | ENSP00000245907.4:p.Gly578Arg | |
ENST00000245907.10:c.1732G>A | ENSP00000245907.4:p.Gly578Arg | |
ENST00000600763.1:n.365G>A | ||
NM_000064.3:c.1732G>A | NP_000055.2:p.Gly578Arg | |
NM_000064.4:c.1732G>A MANE Select | NP_000055.2:p.Gly578Arg |