HGVS | Genome Assembly |
---|---|
NC_000003.12:g.49122769C>G , CM000665.2:g.49122769C>G | GRCh38 |
NC_000003.11:g.49160202C>G , CM000665.1:g.49160202C>G | GRCh37 |
NC_000003.10:g.49135206C>G | NCBI36 |
NG_008094.1:g.15398G>C | |
NG_054716.1:g.3170G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305544.9:c.4508G>C MANE Select | ENSP00000307156.4:p.Gly1503Ala | |
ENST00000305544.8:c.4508G>C | ENSP00000307156.4:p.Gly1503Ala | |
ENST00000418109.5:c.4508G>C | ENSP00000388325.1:p.Gly1503Ala | |
ENST00000469665.1:n.817G>C | ||
NM_002292.3:c.4508G>C | NP_002283.3:p.Gly1503Ala | |
XM_005265127.3:c.4508G>C | XP_005265184.1:p.Gly1503Ala | |
XM_005265127.4:c.4508G>C | XP_005265184.1:p.Gly1503Ala | |
NM_002292.4:c.4508G>C MANE Select | NP_002283.3:p.Gly1503Ala |