HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713231C>A , CM000681.2:g.6713231C>A | GRCh38 |
NC_000019.9:g.6713242C>A , CM000681.1:g.6713242C>A | GRCh37 |
NC_000019.8:g.6664242C>A | NCBI36 |
NG_009557.1:g.12421G>T , LRG_27:g.12421G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.838G>T | ENSP00000512083.1:p.Gly280Trp | |
ENST00000695654.1:c.85G>T | ENSP00000512085.1:p.Gly29Trp | |
ENST00000695692.1:n.285G>T | ||
ENST00000245907.11:c.961G>T MANE Select | ENSP00000245907.4:p.Gly321Trp | |
ENST00000245907.10:c.961G>T | ENSP00000245907.4:p.Gly321Trp | |
ENST00000594270.5:n.85G>T | ||
ENST00000595577.1:n.465G>T | ||
ENST00000597442.5:n.211G>T | ||
NM_000064.3:c.961G>T | NP_000055.2:p.Gly321Trp | |
NM_000064.4:c.961G>T MANE Select | NP_000055.2:p.Gly321Trp |