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Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.103100393C>A , CM000676.2:g.103100393C>A
GRCh38
NC_000014.8:g.103566730C>A , CM000676.1:g.103566730C>A
GRCh37
NC_000014.7:g.102636483C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000687959.1:c.174C>A
ENSP00000508483.1:p.Ser58=
ENST00000688303.1:c.174C>A
MANE Select
ENSP00000509130.1:p.Ser58=
ENST00000380069.7:c.174C>A
ENSP00000369409.3:p.Ser58=
ENST00000559116.1:c.66C>A
ENSP00000454163.1:p.Ser22=
NM_001077594.1:c.174C>A
NP_001071062.1:p.Ser58=
XM_011537323.1:c.348C>A
XP_011535625.1:p.Ser116=
XM_011537324.1:c.348C>A
XP_011535626.1:p.Ser116=
XM_011537325.1:c.174C>A
XP_011535627.1:p.Ser58=
XM_011537326.1:c.174C>A
XP_011535628.1:p.Ser58=
XM_011537327.1:c.174C>A
XP_011535629.1:p.Ser58=
XM_011537328.1:c.174C>A
XP_011535630.1:p.Ser58=
XM_011537329.1:c.174C>A
XP_011535631.1:p.Ser58=
XM_011537330.1:c.174C>A
XP_011535632.1:p.Ser58=
XM_011537331.1:c.174C>A
XP_011535633.1:p.Ser58=
XM_011537332.1:c.174C>A
XP_011535634.1:p.Ser58=
XM_011537333.1:c.285C>A
XP_011535635.1:p.Ser95=
XR_943558.1:n.903C>A
XM_011537323.3:c.348C>A
XP_011535625.1:p.Ser116=
XM_011537324.2:c.348C>A
XP_011535626.1:p.Ser116=
XM_011537325.2:c.174C>A
XP_011535627.1:p.Ser58=
XM_011537327.2:c.174C>A
XP_011535629.1:p.Ser58=
XM_011537328.2:c.174C>A
XP_011535630.1:p.Ser58=
XM_011537329.2:c.174C>A
XP_011535631.1:p.Ser58=
XM_011537330.2:c.174C>A
XP_011535632.1:p.Ser58=
XM_011537332.2:c.174C>A
XP_011535634.1:p.Ser58=
XM_011537333.2:c.285C>A
XP_011535635.1:p.Ser95=
XR_943558.2:n.930C>A
NM_001077594.2:c.174C>A
MANE Select
NP_001071062.1:p.Ser58=
NM_001394941.1:c.174C>A
NP_001381870.1:p.Ser58=
NM_001394942.1:c.174C>A
NP_001381871.1:p.Ser58=