Canonical Allele Identifier: CA378120712

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038717145
• MyVariant Identifiers: chr10:g.101590138G>C (hg19) ; chr10:g.99830381G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830381G>C , CM000672.2:g.99830381G>C	GRCh38
NC_000010.10:g.101590138G>C , CM000672.1:g.101590138G>C	GRCh37
NC_000010.9:g.101580128G>C	NCBI36
NG_011798.1:g.52676G>C
NG_011798.2:g.52784G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2695G>C MANE Select	ENSP00000497274.1:p.Ala899Pro
ENST00000370449.8:c.2695G>C	ENSP00000359478.4:p.Ala899Pro
NM_000392.4:c.2695G>C	NP_000383.1:p.Ala899Pro
XM_006717630.2:c.1999G>C	XP_006717693.1:p.Ala667Pro
XM_006717631.2:c.*122G>C	XP_006717694.1:n.*122G>C
XM_011539291.1:c.2695G>C	XP_011537593.1:p.Ala899Pro
XR_945604.1:n.2884G>C
XR_945605.1:n.2886G>C
NM_000392.5:c.2695G>C MANE Select	NP_000383.2:p.Ala899Pro
XM_006717630.3:c.1999G>C	XP_006717693.1:p.Ala667Pro
XM_006717631.4:c.*122G>C	XP_006717694.1:n.*122G>C
XM_011539291.3:c.2695G>C	XP_011537593.1:p.Ala899Pro
XR_945604.3:n.2938G>C
XR_945605.3:n.2938G>C