Canonical Allele Identifier: CA1931489174

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830381G= , CM000672.2:g.99830381G=	GRCh38
NC_000010.10:g.101590138G= , CM000672.1:g.101590138G=	GRCh37
NC_000010.9:g.101580128G=	NCBI36
NG_011798.1:g.52676G=
NG_011798.2:g.52784G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2695G= MANE Select	ENSP00000497274.1:p.Ala899=
ENST00000370449.8:c.2695G=	ENSP00000359478.4:p.Ala899=
NM_000392.4:c.2695G=	NP_000383.1:p.Ala899=
XM_006717630.2:c.1999G=	XP_006717693.1:p.Ala667=
XM_006717631.2:c.*122G=	XP_006717694.1:n.*122G=
XM_011539291.1:c.2695G=	XP_011537593.1:p.Ala899=
XR_945604.1:n.2884G=
XR_945605.1:n.2886G=
NM_000392.5:c.2695G= MANE Select	NP_000383.2:p.Ala899=
XM_006717630.3:c.1999G=	XP_006717693.1:p.Ala667=
XM_006717631.4:c.*122G=	XP_006717694.1:n.*122G=
XM_011539291.3:c.2695G=	XP_011537593.1:p.Ala899=
XR_945604.3:n.2938G=
XR_945605.3:n.2938G=