Canonical Allele Identifier: CA1931511972

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844391T= , CM000672.2:g.99844391T=	GRCh38
NC_000010.10:g.101604148T= , CM000672.1:g.101604148T=	GRCh37
NC_000010.9:g.101594138T=	NCBI36
NG_011798.1:g.66686T=
NG_011798.2:g.66794T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3913T= MANE Select	ENSP00000497274.1:p.Tyr1305=
ENST00000649459.1:n.261T=
ENST00000370449.8:c.3913T=	ENSP00000359478.4:p.Tyr1305=
NM_000392.4:c.3913T=	NP_000383.1:p.Tyr1305=
XM_006717630.2:c.3217T=	XP_006717693.1:p.Tyr1073=
XR_945604.1:n.4102T=
XR_945605.1:n.3977T=
NM_000392.5:c.3913T= MANE Select	NP_000383.2:p.Tyr1305=
XM_006717630.3:c.3217T=	XP_006717693.1:p.Tyr1073=
XR_945604.3:n.4156T=
XR_945605.3:n.4029T=