Canonical Allele Identifier: CA1931512132

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038989130

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844471T>C , CM000672.2:g.99844471T>C	GRCh38
NC_000010.10:g.101604228T>C , CM000672.1:g.101604228T>C	GRCh37
NC_000010.9:g.101594218T>C	NCBI36
NG_011798.1:g.66766T>C
NG_011798.2:g.66874T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3987+6T>C MANE Select	ENSP00000497274.1:n.3987+6T>C
ENST00000649459.1:n.335+6T>C
ENST00000370449.8:c.3987+6T>C	ENSP00000359478.4:n.3987+6T>C
NM_000392.4:c.3987+6T>C	NP_000383.1:n.3987+6T>C
XM_006717630.2:c.3291+6T>C	XP_006717693.1:n.3291+6T>C
XR_945604.1:n.4176+6T>C
XR_945605.1:n.4051+6T>C
NM_000392.5:c.3987+6T>C MANE Select	NP_000383.2:n.3987+6T>C
XM_006717630.3:c.3291+6T>C	XP_006717693.1:n.3291+6T>C
XR_945604.3:n.4230+6T>C
XR_945605.3:n.4103+6T>C