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Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.50242548G>T , CM000677.2:g.50242548G>T
GRCh38
NC_000015.9:g.50534745G>T , CM000677.1:g.50534745G>T
GRCh37
NC_000015.8:g.48322037G>T
NCBI36
NG_027487.1:g.28418C>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000267845.8:c.1701C>A
MANE Select
ENSP00000267845.3:p.Ser567=
ENST00000267845.7:c.1701C>A
ENSP00000267845.3:p.Ser567=
ENST00000543581.5:c.1602C>A
ENSP00000440252.1:p.Ser534=
ENST00000559816.1:n.1445C>A
NM_001306146.1:c.1602C>A
NP_001293075.1:p.Ser534=
NM_002112.3:c.1701C>A
NP_002103.2:p.Ser567=
XM_011521479.1:c.1464C>A
XP_011519781.1:p.Ser488=
XM_011521480.1:c.1269C>A
XP_011519782.1:p.Ser423=
XM_017022094.1:c.1806C>A
XP_016877583.1:p.Ser602=
XM_017022095.1:c.1707C>A
XP_016877584.1:p.Ser569=
XM_017022096.1:c.1578C>A
XP_016877585.1:p.Ser526=
XM_017022097.1:c.1569C>A
XP_016877586.1:p.Ser523=
XM_017022098.1:c.1374C>A
XP_016877587.1:p.Ser458=
NM_002112.4:c.1701C>A
MANE Select
NP_002103.2:p.Ser567=
NM_001306146.2:c.1602C>A
NP_001293075.1:p.Ser534=