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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.173909613C>T , CM000663.2:g.173909613C>T
GRCh38
NC_000001.10:g.173878751C>T , CM000663.1:g.173878751C>T
GRCh37
NC_000001.9:g.172145374C>T
NCBI36
NG_012462.1:g.12766G>A , LRG_577:g.12766G>A
Transcript Alleles
HGVS
Amino-acid Change
ENST00000367698.4:c.1092G>A
MANE Select
ENSP00000356671.3:p.Lys364=
ENST00000367698.3:c.1092G>A
ENSP00000356671.3:p.Lys364=
ENST00000617423.4:c.560-2120G>A
ENSP00000478688.1:n.560-2120G>A
NM_000488.3:c.1092G>A , LRG_577t1:c.1092G>A
NP_000479.1:p.Lys364=
XM_005245198.2:c.948G>A
XP_005245255.1:p.Lys316=
NM_001365052.1:c.948G>A
NP_001351981.1:p.Lys316=
NM_000488.4:c.1092G>A
MANE Select
NP_000479.1:p.Lys364=
NM_001365052.2:c.948G>A
NP_001351981.1:p.Lys316=
NM_001386302.1:c.1215G>A
NP_001373231.1:p.Lys405=
NM_001386303.1:c.1173G>A
NP_001373232.1:p.Lys391=
NM_001386304.1:c.1071G>A
NP_001373233.1:p.Lys357=
NM_001386305.1:c.1035G>A
NP_001373234.1:p.Lys345=
NM_001386306.1:c.876G>A
NP_001373235.1:p.Lys292=