Canonical Allele Identifier: CA471131624

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99782756-G-C
• MyVariant Identifiers: chr10:g.101542513G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99782756G>C , CM000672.2:g.99782756G>C	GRCh38
NC_000010.10:g.101542513G>C , CM000672.1:g.101542513G>C	GRCh37
NC_000010.9:g.101532503G>C	NCBI36
NG_011798.1:g.5051G>C
NG_011798.2:g.5159G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.-89G>C MANE Select	ENSP00000497274.1:n.-89G>C
ENST00000647836.1:n.117G>C
ENST00000648324.1:c.-89G>C	ENSP00000497248.1:n.-89G>C
ENST00000648689.1:c.-89G>C	ENSP00000496972.1:n.-89G>C
ENST00000649932.1:c.-89G>C	ENSP00000498120.1:n.-89G>C
ENST00000370449.8:c.-89G>C	ENSP00000359478.4:n.-89G>C
NM_000392.4:c.-89G>C	NP_000383.1:n.-89G>C
XM_006717631.2:c.-89G>C	XP_006717694.1:n.-89G>C
XM_011539291.1:c.-89G>C	XP_011537593.1:n.-89G>C
XR_945604.1:n.101G>C
XR_945605.1:n.103G>C
NM_000392.5:c.-89G>C MANE Select	NP_000383.2:n.-89G>C
XM_006717631.4:c.-89G>C	XP_006717694.1:n.-89G>C
XM_011539291.3:c.-89G>C	XP_011537593.1:n.-89G>C
XM_017015675.2:c.-89G>C	XP_016871164.1:n.-89G>C
XR_945604.3:n.155G>C
XR_945605.3:n.155G>C