Canonical Allele Identifier: CA670643606

Gene: ABCC2

Linked Data

• dbSNP Id: rs1357337871
• gnomAD v3: 10-99782726-C-T
• gnomAD v4: 10-99782726-C-T
• MyVariant Identifiers: chr10:g.101542483C>T (hg19) ; chr10:g.99782726C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99782726C>T , CM000672.2:g.99782726C>T	GRCh38
NC_000010.10:g.101542483C>T , CM000672.1:g.101542483C>T	GRCh37
NC_000010.9:g.101532473C>T	NCBI36
NG_011798.1:g.5021C>T
NG_011798.2:g.5129C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.-119C>T MANE Select	ENSP00000497274.1:n.-119C>T
ENST00000647836.1:n.87C>T
ENST00000648324.1:c.-119C>T	ENSP00000497248.1:n.-119C>T
ENST00000648689.1:c.-119C>T	ENSP00000496972.1:n.-119C>T
ENST00000649932.1:c.-119C>T	ENSP00000498120.1:n.-119C>T
NM_000392.4:c.-119C>T	NP_000383.1:n.-119C>T
XM_006717631.2:c.-119C>T	XP_006717694.1:n.-119C>T
XM_011539291.1:c.-119C>T	XP_011537593.1:n.-119C>T
XR_945604.1:n.71C>T
XR_945605.1:n.73C>T
NM_000392.5:c.-119C>T MANE Select	NP_000383.2:n.-119C>T
XM_006717631.4:c.-119C>T	XP_006717694.1:n.-119C>T
XM_011539291.3:c.-119C>T	XP_011537593.1:n.-119C>T
XM_017015675.2:c.-119C>T	XP_016871164.1:n.-119C>T
XR_945604.3:n.125C>T
XR_945605.3:n.125C>T