Canonical Allele Identifier: CA1931496044

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99836099T= , CM000672.2:g.99836099T=	GRCh38
NC_000010.10:g.101595856T= , CM000672.1:g.101595856T=	GRCh37
NC_000010.9:g.101585846T=	NCBI36
NG_011798.1:g.58394T=
NG_011798.2:g.58502T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3423T= MANE Select	ENSP00000497274.1:p.Tyr1141=
ENST00000370449.8:c.3423T=	ENSP00000359478.4:p.Tyr1141=
NM_000392.4:c.3423T=	NP_000383.1:p.Tyr1141=
XM_006717630.2:c.2727T=	XP_006717693.1:p.Tyr909=
XR_945604.1:n.3612T=
XR_945605.1:n.3614T=
NM_000392.5:c.3423T= MANE Select	NP_000383.2:p.Tyr1141=
XM_006717630.3:c.2727T=	XP_006717693.1:p.Tyr909=
XR_945604.3:n.3666T=
XR_945605.3:n.3666T=