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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.111122134T>A , CM000665.2:g.111122134T>A
GRCh38
NC_000003.11:g.110840981T>A , CM000665.1:g.110840981T>A
GRCh37
NC_000003.10:g.112323671T>A
NCBI36
NG_029835.1:g.55376T>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000485303.6:c.813T>A
MANE Select
ENSP00000418070.1:p.Val271=
ENST00000319792.7:c.813T>A
ENSP00000321514.3:p.Val271=
ENST00000485303.5:c.813T>A
ENSP00000418070.1:p.Val271=
ENST00000486596.5:c.514T>A
ENST00000493615.5:c.744T>A
ENSP00000420579.1:p.Val248=
NM_001243286.1:c.813T>A
NP_001230215.1:p.Val271=
NM_001243288.1:c.744T>A
NP_001230217.1:p.Val248=
NM_015480.2:c.813T>A
NP_056295.1:p.Val271=
XM_005247322.3:c.813T>A
XP_005247379.2:p.Val271=
XM_011512662.1:c.906T>A
XP_011510964.1:p.Val302=
XM_011512663.1:c.906T>A
XP_011510965.1:p.Val302=
XM_011512664.1:c.744T>A
XP_011510966.1:p.Val248=
XM_011512665.1:c.906T>A
XP_011510967.1:p.Val302=
XM_011512666.1:c.906T>A
XP_011510968.1:p.Val302=
XM_011512667.1:c.177T>A
XP_011510969.1:p.Val59=
XR_924122.1:n.1136T>A
XM_017006123.1:c.906T>A
XP_016861612.1:p.Val302=
XM_017006124.1:c.768T>A
XP_016861613.1:p.Val256=
XM_017006125.1:c.744T>A
XP_016861614.1:p.Val248=
XM_017006126.1:c.813T>A
XP_016861615.1:p.Val271=
XM_017006127.2:c.177T>A
XP_016861616.1:p.Val59=
XR_002959508.1:n.1094T>A
XR_924122.2:n.1136T>A
NM_015480.3:c.813T>A
MANE Select
NP_056295.1:p.Val271=
NM_001243286.2:c.813T>A
NP_001230215.1:p.Val271=
NM_001243288.2:c.744T>A
NP_001230217.1:p.Val248=