HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6718376G>C , CM000681.2:g.6718376G>C | GRCh38 |
NC_000019.9:g.6718387G>C , CM000681.1:g.6718387G>C | GRCh37 |
NC_000019.8:g.6669387G>C | NCBI36 |
NG_009557.1:g.7276C>G , LRG_27:g.7276C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000594936.2:n.365C>G | ||
ENST00000695652.1:c.181C>G | ENSP00000512083.1:p.Arg61Gly | |
ENST00000695693.1:c.304C>G | ENSP00000512104.1:p.Arg102Gly | |
ENST00000245907.11:c.304C>G MANE Select | ENSP00000245907.4:p.Arg102Gly | |
ENST00000245907.10:c.304C>G | ENSP00000245907.4:p.Arg102Gly | |
ENST00000594936.1:n.365C>G | ||
ENST00000600744.1:c.181C>G | ENSP00000472044.1:p.Arg61Gly | |
NM_000064.3:c.304C>G | NP_000055.2:p.Arg102Gly | |
NM_000064.4:c.304C>G MANE Select | NP_000055.2:p.Arg102Gly |