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Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.76469802C>A , CM000679.2:g.76469802C>A
GRCh38
NC_000017.10:g.74465884C>A , CM000679.1:g.74465884C>A
GRCh37
NC_000017.9:g.71977479C>A
NCBI36
NG_015976.1:g.21452C>A
NG_032852.1:g.36626G>T , LRG_532:g.36626G>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000392492.8:c.456C>A
MANE Select
ENSP00000376282.2:p.Ala152=
ENST00000250615.7:c.591C>A
ENSP00000250615.2:p.Ala197=
ENST00000392492.7:c.456C>A
ENSP00000376282.2:p.Ala152=
ENST00000587798.1:c.*233C>A
ENSP00000468239.1:n.*233C>A
NM_001088.2:c.456C>A
NP_001079.1:p.Ala152=
NM_001166579.1:c.591C>A
NP_001160051.1:p.Ala197=
NR_110548.1:n.767C>A
XM_011524415.1:c.456C>A
XP_011522717.1:p.Ala152=
XM_011524416.1:c.663C>A
XP_011522718.1:p.Ala221=
XM_011524417.1:c.663C>A
XP_011522719.1:p.Ala221=
XM_011524418.1:c.663C>A
XP_011522720.1:p.Ala221=
XM_011524419.1:c.663C>A
XP_011522721.1:p.Ala221=
XM_011524420.1:c.663C>A
XP_011522722.1:p.Ala221=
XM_011524421.1:c.663C>A
XP_011522723.1:p.Ala221=
XM_011524422.1:c.546C>A
XP_011522724.1:p.Ala182=
XM_011524423.1:c.456C>A
XP_011522725.1:p.Ala152=
XM_017024259.1:c.570C>A
XP_016879748.1:p.Ala190=
NM_001088.3:c.456C>A
MANE Select
NP_001079.1:p.Ala152=
NR_110548.2:n.712C>A
NM_001166579.2:c.591C>A
NP_001160051.1:p.Ala197=