Canonical Allele Identifier: CA212857629

Gene: ABCC2

Linked Data

• dbSNP Id: rs1018118131
• MyVariant Identifiers: chr10:g.101590059C>G (hg19) ; chr10:g.99830302C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830302C>G , CM000672.2:g.99830302C>G	GRCh38
NC_000010.10:g.101590059C>G , CM000672.1:g.101590059C>G	GRCh37
NC_000010.9:g.101580049C>G	NCBI36
NG_011798.1:g.52597C>G
NG_011798.2:g.52705C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2621-5C>G MANE Select	ENSP00000497274.1:n.2621-5C>G
ENST00000370449.8:c.2621-5C>G	ENSP00000359478.4:n.2621-5C>G
NM_000392.4:c.2621-5C>G	NP_000383.1:n.2621-5C>G
XM_006717630.2:c.1925-5C>G	XP_006717693.1:n.1925-5C>G
XM_006717631.2:c.*48-5C>G	XP_006717694.1:n.*48-5C>G
XM_011539291.1:c.2621-5C>G	XP_011537593.1:n.2621-5C>G
XR_945604.1:n.2810-5C>G
XR_945605.1:n.2812-5C>G
NM_000392.5:c.2621-5C>G MANE Select	NP_000383.2:n.2621-5C>G
XM_006717630.3:c.1925-5C>G	XP_006717693.1:n.1925-5C>G
XM_006717631.4:c.*48-5C>G	XP_006717694.1:n.*48-5C>G
XM_011539291.3:c.2621-5C>G	XP_011537593.1:n.2621-5C>G
XR_945604.3:n.2864-5C>G
XR_945605.3:n.2864-5C>G