Canonical Allele Identifier: CA1931513941

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845695T= , CM000672.2:g.99845695T=	GRCh38
NC_000010.10:g.101605452T= , CM000672.1:g.101605452T=	GRCh37
NC_000010.9:g.101595442T=	NCBI36
NG_011798.1:g.67990T=
NG_011798.2:g.68098T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4059T= MANE Select	ENSP00000497274.1:p.Ala1353=
ENST00000649459.1:n.407T=
ENST00000370449.8:c.4059T=	ENSP00000359478.4:p.Ala1353=
NM_000392.4:c.4059T=	NP_000383.1:p.Ala1353=
XM_006717630.2:c.3363T=	XP_006717693.1:p.Ala1121=
XR_945604.1:n.4189T=
XR_945605.1:n.4123T=
NM_000392.5:c.4059T= MANE Select	NP_000383.2:p.Ala1353=
XM_006717630.3:c.3363T=	XP_006717693.1:p.Ala1121=
XR_945604.3:n.4243T=
XR_945605.3:n.4175T=