Canonical Allele Identifier: CA1931489631

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038721845

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830613T>G , CM000672.2:g.99830613T>G	GRCh38
NC_000010.10:g.101590370T>G , CM000672.1:g.101590370T>G	GRCh37
NC_000010.9:g.101580360T>G	NCBI36
NG_011798.1:g.52908T>G
NG_011798.2:g.53016T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-103T>G MANE Select	ENSP00000497274.1:n.2748-103T>G
ENST00000370449.8:c.2748-103T>G	ENSP00000359478.4:n.2748-103T>G
NM_000392.4:c.2748-103T>G	NP_000383.1:n.2748-103T>G
XM_006717630.2:c.2052-103T>G	XP_006717693.1:n.2052-103T>G
XM_011539291.1:c.2747+180T>G	XP_011537593.1:n.2747+180T>G
XR_945604.1:n.2937-103T>G
XR_945605.1:n.2939-103T>G
NM_000392.5:c.2748-103T>G MANE Select	NP_000383.2:n.2748-103T>G
XM_006717630.3:c.2052-103T>G	XP_006717693.1:n.2052-103T>G
XM_011539291.3:c.2747+180T>G	XP_011537593.1:n.2747+180T>G
XR_945604.3:n.2991-103T>G
XR_945605.3:n.2991-103T>G