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Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.98707657A= , CM000677.2:g.98707657A=
GRCh38
NC_000015.9:g.99250886A= , CM000677.1:g.99250886A=
GRCh37
NC_000015.8:g.97068409A=
NCBI36
NG_009492.1:g.63126A=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000649865.1:c.190A=
ENSP00000496919.1:p.Ile64=
ENST00000650285.1:c.190A=
MANE Select
ENSP00000497069.1:p.Ile64=
ENST00000268035.10:c.190A=
ENSP00000268035.6:p.Ile64=
ENST00000558762.5:c.190A=
ENSP00000453007.1:p.Ile64=
ENST00000559925.5:n.190A=
NM_000875.4:c.190A=
NP_000866.1:p.Ile64=
NM_001291858.1:c.190A=
NP_001278787.1:p.Ile64=
XM_011521513.1:c.190A=
XP_011519815.1:p.Ile64=
XM_011521514.1:c.190A=
XP_011519816.1:p.Ile64=
XM_011521515.1:c.190A=
XP_011519817.1:p.Ile64=
XM_017022136.1:c.265A=
XP_016877625.1:p.Ile89=
XM_017022137.1:c.265A=
XP_016877626.1:p.Ile89=
XM_017022138.1:c.265A=
XP_016877627.1:p.Ile89=
XM_017022139.1:c.-174A=
XP_016877628.1:n.-174A=
NM_000875.5:c.190A=
MANE Select
NP_000866.1:p.Ile64=
NM_001291858.2:c.190A=
NP_001278787.1:p.Ile64=