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Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.3793444T>A , CM000678.2:g.3793444T>A
GRCh38
NC_000016.9:g.3843445T>A , CM000678.1:g.3843445T>A
GRCh37
NC_000016.8:g.3783446T>A
NCBI36
NG_009873.1:g.91677A>T
NG_009873.2:g.92270A>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000262367.10:c.1158A>T
MANE Select
ENSP00000262367.5:p.Arg386=
ENST00000262367.9:c.1158A>T
ENSP00000262367.5:p.Arg386=
ENST00000382070.7:c.1158A>T
ENSP00000371502.3:p.Arg386=
NM_001079846.1:c.1158A>T
NP_001073315.1:p.Arg386=
NM_004380.2:c.1158A>T
NP_004371.2:p.Arg386=
XM_005255124.3:c.1158A>T
XP_005255181.1:p.Arg386=
XM_005255125.3:c.1158A>T
XP_005255182.1:p.Arg386=
XM_006720848.2:c.1158A>T
XP_006720911.1:p.Arg386=
XM_011522380.1:c.1104A>T
XP_011520682.1:p.Arg368=
XM_011522381.1:c.405A>T
XP_011520683.1:p.Arg135=
XM_011522382.1:c.1158A>T
XP_011520684.1:p.Arg386=
XM_005255124.4:c.1158A>T
XP_005255181.1:p.Arg386=
XM_005255125.4:c.1158A>T
XP_005255182.1:p.Arg386=
XM_006720848.3:c.1158A>T
XP_006720911.1:p.Arg386=
XM_011522381.2:c.405A>T
XP_011520683.1:p.Arg135=
XM_011522382.3:c.1158A>T
XP_011520684.1:p.Arg386=
XM_017022944.1:c.1158A>T
XP_016878433.1:p.Arg386=
NM_004380.3:c.1158A>T
MANE Select
NP_004371.2:p.Arg386=