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Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.12915894T>G , CM000686.2:g.12915894T>G
GRCh38
NC_000024.9:g.15027806T>G , CM000686.1:g.15027806T>G
GRCh37
NC_000024.8:g.13537200T>G
NCBI36
NG_012831.1:g.16788T>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000336079.8:c.1176T>G
MANE Select
ENSP00000336725.3:p.Arg392=
ENST00000336079.7:c.1176T>G
ENSP00000336725.3:p.Arg392=
ENST00000360160.8:c.1176T>G
ENSP00000353284.4:p.Arg392=
ENST00000495478.1:n.291T>G
NM_001122665.2:c.1176T>G
NP_001116137.1:p.Arg392=
NM_001302552.1:c.1167T>G
NP_001289481.1:p.Arg389=
NM_004660.4:c.1176T>G
NP_004651.2:p.Arg392=
XM_006724878.1:c.1176T>G
XP_006724941.1:p.Arg392=
XM_011531471.1:c.1176T>G
XP_011529773.1:p.Arg392=
NM_001122665.3:c.1176T>G
NP_001116137.1:p.Arg392=
NM_001302552.2:c.1167T>G
NP_001289481.1:p.Arg389=
NM_001324195.1:c.1176T>G
NP_001311124.1:p.Arg392=
NR_136716.1:n.1645T>G
NR_136717.1:n.1407T>G
NR_136718.1:n.1725T>G
NR_136719.1:n.1515T>G
NR_136720.1:n.1645T>G
NR_136721.1:n.1238T>G
NR_136722.1:n.1322T>G
NR_136723.1:n.1640T>G
NR_136724.1:n.1560T>G
XR_001756014.2:n.1280T>G
NM_004660.5:c.1176T>G
MANE Select
NP_004651.2:p.Arg392=
NM_001302552.3:c.1167T>G
NP_001289481.1:p.Arg389=
NM_001324195.2:c.1176T>G
NP_001311124.1:p.Arg392=
NR_136716.2:n.1563T>G
NR_136717.2:n.1325T>G
NR_136718.2:n.1643T>G
NR_136719.2:n.1433T>G
NR_136720.2:n.1563T>G
NR_136721.2:n.1228T>G