Canonical Allele Identifier: CA2610492378

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99782735-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99782735T>C , CM000672.2:g.99782735T>C	GRCh38
NC_000010.10:g.101542492T>C , CM000672.1:g.101542492T>C	GRCh37
NC_000010.9:g.101532482T>C	NCBI36
NG_011798.1:g.5030T>C
NG_011798.2:g.5138T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.-110T>C MANE Select	ENSP00000497274.1:n.-110T>C
ENST00000647836.1:n.96T>C
ENST00000648324.1:c.-110T>C	ENSP00000497248.1:n.-110T>C
ENST00000648689.1:c.-110T>C	ENSP00000496972.1:n.-110T>C
ENST00000649932.1:c.-110T>C	ENSP00000498120.1:n.-110T>C
ENST00000370449.8:c.-110T>C	ENSP00000359478.4:n.-110T>C
NM_000392.4:c.-110T>C	NP_000383.1:n.-110T>C
XM_006717631.2:c.-110T>C	XP_006717694.1:n.-110T>C
XM_011539291.1:c.-110T>C	XP_011537593.1:n.-110T>C
XR_945604.1:n.80T>C
XR_945605.1:n.82T>C
NM_000392.5:c.-110T>C MANE Select	NP_000383.2:n.-110T>C
XM_006717631.4:c.-110T>C	XP_006717694.1:n.-110T>C
XM_011539291.3:c.-110T>C	XP_011537593.1:n.-110T>C
XM_017015675.2:c.-110T>C	XP_016871164.1:n.-110T>C
XR_945604.3:n.134T>C
XR_945605.3:n.134T>C