Canonical Allele Identifier: CA1931511762

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038984673

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844261T>C , CM000672.2:g.99844261T>C	GRCh38
NC_000010.10:g.101604018T>C , CM000672.1:g.101604018T>C	GRCh37
NC_000010.9:g.101594008T>C	NCBI36
NG_011798.1:g.66556T>C
NG_011798.2:g.66664T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3844-61T>C MANE Select	ENSP00000497274.1:n.3844-61T>C
ENST00000649459.1:n.192-61T>C
ENST00000370449.8:c.3844-61T>C	ENSP00000359478.4:n.3844-61T>C
NM_000392.4:c.3844-61T>C	NP_000383.1:n.3844-61T>C
XM_006717630.2:c.3148-61T>C	XP_006717693.1:n.3148-61T>C
XR_945604.1:n.4033-61T>C
XR_945605.1:n.3908-61T>C
NM_000392.5:c.3844-61T>C MANE Select	NP_000383.2:n.3844-61T>C
XM_006717630.3:c.3148-61T>C	XP_006717693.1:n.3148-61T>C
XR_945604.3:n.4087-61T>C
XR_945605.3:n.3960-61T>C