Canonical Allele Identifier: CA1931511721

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844215C= , CM000672.2:g.99844215C=	GRCh38
NC_000010.10:g.101603972C= , CM000672.1:g.101603972C=	GRCh37
NC_000010.9:g.101593962C=	NCBI36
NG_011798.1:g.66510C=
NG_011798.2:g.66618C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-107C= MANE Select	ENSP00000497274.1:n.3844-107C=
ENST00000649459.1:n.192-107C=
ENST00000370449.8:c.3844-107C=	ENSP00000359478.4:n.3844-107C=
NM_000392.4:c.3844-107C=	NP_000383.1:n.3844-107C=
XM_006717630.2:c.3148-107C=	XP_006717693.1:n.3148-107C=
XR_945604.1:n.4033-107C=
XR_945605.1:n.3908-107C=
NM_000392.5:c.3844-107C= MANE Select	NP_000383.2:n.3844-107C=
XM_006717630.3:c.3148-107C=	XP_006717693.1:n.3148-107C=
XR_945604.3:n.4087-107C=
XR_945605.3:n.3960-107C=