Canonical Allele Identifier: CA1388615851

Gene: IMPG2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.101243620C= , CM000665.2:g.101243620C=	GRCh38
NC_000003.11:g.100962464C= , CM000665.1:g.100962464C=	GRCh37
NC_000003.10:g.102445154C=	NCBI36
NG_028284.1:g.81956G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000193391.8:c.2711G= MANE Select	ENSP00000193391.6:p.Ser904=
ENST00000193391.7:c.2711G=	ENSP00000193391.6:p.Ser904=
NM_016247.3:c.2711G=	NP_057331.2:p.Ser904=
XM_011512871.1:c.2417G=	XP_011511173.1:p.Ser806=
XM_011512872.1:c.2300G=	XP_011511174.1:p.Ser767=
NM_016247.4:c.2711G= MANE Select	NP_057331.2:p.Ser904=