Canonical Allele Identifier: CA1931509430

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817413C= , CM000672.2:g.99817413C=	GRCh38
NC_000010.10:g.101577170C= , CM000672.1:g.101577170C=	GRCh37
NC_000010.9:g.101567160C=	NCBI36
NG_011798.1:g.39708C=
NG_011798.2:g.39816C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2200C= MANE Select	ENSP00000497274.1:p.Leu734=
ENST00000370449.8:c.2200C=	ENSP00000359478.4:p.Leu734=
NM_000392.4:c.2200C=	NP_000383.1:p.Leu734=
XM_006717630.2:c.1504C=	XP_006717693.1:p.Leu502=
XM_006717631.2:c.2200C=	XP_006717694.1:p.Leu734=
XM_011539291.1:c.2200C=	XP_011537593.1:p.Leu734=
XR_945604.1:n.2389C=
XR_945605.1:n.2391C=
NM_000392.5:c.2200C= MANE Select	NP_000383.2:p.Leu734=
XM_006717630.3:c.1504C=	XP_006717693.1:p.Leu502=
XM_006717631.4:c.2200C=	XP_006717694.1:p.Leu734=
XM_011539291.3:c.2200C=	XP_011537593.1:p.Leu734=
XM_017015675.2:c.2200C=	XP_016871164.1:p.Leu734=
XR_945604.3:n.2443C=
XR_945605.3:n.2443C=