Canonical Allele Identifier: CA2789199764

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844572A>C , CM000672.2:g.99844572A>C	GRCh38
NC_000010.10:g.101604329A>C , CM000672.1:g.101604329A>C	GRCh37
NC_000010.9:g.101594319A>C	NCBI36
NG_011798.1:g.66867A>C
NG_011798.2:g.66975A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3987+107A>C MANE Select	ENSP00000497274.1:n.3987+107A>C
ENST00000649459.1:n.335+107A>C
ENST00000370449.8:c.3987+107A>C	ENSP00000359478.4:n.3987+107A>C
NM_000392.4:c.3987+107A>C	NP_000383.1:n.3987+107A>C
XM_006717630.2:c.3291+107A>C	XP_006717693.1:n.3291+107A>C
XR_945604.1:n.4176+107A>C
XR_945605.1:n.4051+107A>C
NM_000392.5:c.3987+107A>C MANE Select	NP_000383.2:n.3987+107A>C
XM_006717630.3:c.3291+107A>C	XP_006717693.1:n.3291+107A>C
XR_945604.3:n.4230+107A>C
XR_945605.3:n.4103+107A>C