Canonical Allele Identifier: CA1931509206

Gene: ABCC2

Linked Data

• ClinVar Variation Id: 2961283
• ClinVar RCV Id: RCV003819994
• dbSNP Id: rs1564687750
• gnomAD v4: 10-99817289-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817289C>A , CM000672.2:g.99817289C>A	GRCh38
NC_000010.10:g.101577046C>A , CM000672.1:g.101577046C>A	GRCh37
NC_000010.9:g.101567036C>A	NCBI36
NG_011798.1:g.39584C>A
NG_011798.2:g.39692C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2095-19C>A MANE Select	ENSP00000497274.1:n.2095-19C>A
ENST00000370449.8:c.2095-19C>A	ENSP00000359478.4:n.2095-19C>A
NM_000392.4:c.2095-19C>A	NP_000383.1:n.2095-19C>A
XM_006717630.2:c.1399-19C>A	XP_006717693.1:n.1399-19C>A
XM_006717631.2:c.2095-19C>A	XP_006717694.1:n.2095-19C>A
XM_011539291.1:c.2095-19C>A	XP_011537593.1:n.2095-19C>A
XR_945604.1:n.2284-19C>A
XR_945605.1:n.2286-19C>A
NM_000392.5:c.2095-19C>A MANE Select	NP_000383.2:n.2095-19C>A
XM_006717630.3:c.1399-19C>A	XP_006717693.1:n.1399-19C>A
XM_006717631.4:c.2095-19C>A	XP_006717694.1:n.2095-19C>A
XM_011539291.3:c.2095-19C>A	XP_011537593.1:n.2095-19C>A
XM_017015675.2:c.2095-19C>A	XP_016871164.1:n.2095-19C>A
XR_945604.3:n.2338-19C>A
XR_945605.3:n.2338-19C>A