Canonical Allele Identifier: CA471261829

Gene: ABCC2

Linked Data

• ClinVar Variation Id: 2962849
• ClinVar RCV Id: RCV003827959
• dbSNP Id: rs1390911775
• gnomAD v2: 10-101578594-A-G
• gnomAD v3: 10-99818837-A-G
• gnomAD v4: 10-99818837-A-G
• MyVariant Identifiers: chr10:g.101578594A>G (hg19) ; chr10:g.99818837A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99818837A>G , CM000672.2:g.99818837A>G	GRCh38
NC_000010.10:g.101578594A>G , CM000672.1:g.101578594A>G	GRCh37
NC_000010.9:g.101568584A>G	NCBI36
NG_011798.1:g.41132A>G
NG_011798.2:g.41240A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2319A>G MANE Select	ENSP00000497274.1:p.Arg773=
ENST00000370449.8:c.2319A>G	ENSP00000359478.4:p.Arg773=
NM_000392.4:c.2319A>G	NP_000383.1:p.Arg773=
XM_006717630.2:c.1623A>G	XP_006717693.1:p.Arg541=
XM_006717631.2:c.2319A>G	XP_006717694.1:p.Arg773=
XM_011539291.1:c.2319A>G	XP_011537593.1:p.Arg773=
XR_945604.1:n.2508A>G
XR_945605.1:n.2510A>G
NM_000392.5:c.2319A>G MANE Select	NP_000383.2:p.Arg773=
XM_006717630.3:c.1623A>G	XP_006717693.1:p.Arg541=
XM_006717631.4:c.2319A>G	XP_006717694.1:p.Arg773=
XM_011539291.3:c.2319A>G	XP_011537593.1:p.Arg773=
XM_017015675.2:c.2319A>G	XP_016871164.1:p.Arg773=
XR_945604.3:n.2562A>G
XR_945605.3:n.2562A>G