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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.12192930C>A , CM000663.2:g.12192930C>A
GRCh38
NC_000001.10:g.12252987C>A , CM000663.1:g.12252987C>A
GRCh37
NC_000001.9:g.12175574C>A
NCBI36
NG_029791.1:g.30928C>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000376259.7:c.619C>A
MANE Select
ENSP00000365435.3:p.Arg207=
ENST00000376259.6:c.619C>A
ENSP00000365435.3:p.Arg207=
ENST00000489921.1:n.331C>A
ENST00000492361.1:n.608C>A
NM_001066.2:c.619C>A
NP_001057.1:p.Arg207=
XM_011542060.1:c.619C>A
XP_011540362.1:p.Arg207=
XM_011542061.1:c.619C>A
XP_011540363.1:p.Arg207=
XM_011542062.1:c.598C>A
XP_011540364.1:p.Arg200=
XM_011542063.1:c.619C>A
XP_011540365.1:p.Arg207=
XM_011542060.2:c.619C>A
XP_011540362.1:p.Arg207=
XM_011542063.2:c.619C>A
XP_011540365.1:p.Arg207=
XM_017002211.1:c.619C>A
XP_016857700.1:p.Arg207=
XM_017002214.1:c.34C>A
XP_016857703.1:p.Arg12=
XM_017002215.1:c.34C>A
XP_016857704.1:p.Arg12=
NM_001066.3:c.619C>A
MANE Select
NP_001057.1:p.Arg207=