Canonical Allele Identifier: CA378128118

Gene: ABCC2

Linked Data

• dbSNP Id: rs1590192950
• MyVariant Identifiers: chr10:g.101605454C>G (hg19) ; chr10:g.99845697C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845697C>G , CM000672.2:g.99845697C>G	GRCh38
NC_000010.10:g.101605454C>G , CM000672.1:g.101605454C>G	GRCh37
NC_000010.9:g.101595444C>G	NCBI36
NG_011798.1:g.67992C>G
NG_011798.2:g.68100C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4061C>G MANE Select	ENSP00000497274.1:p.Ala1354Gly
ENST00000649459.1:n.409C>G
ENST00000370449.8:c.4061C>G	ENSP00000359478.4:p.Ala1354Gly
NM_000392.4:c.4061C>G	NP_000383.1:p.Ala1354Gly
XM_006717630.2:c.3365C>G	XP_006717693.1:p.Ala1122Gly
XR_945604.1:n.4191C>G
XR_945605.1:n.4125C>G
NM_000392.5:c.4061C>G MANE Select	NP_000383.2:p.Ala1354Gly
XM_006717630.3:c.3365C>G	XP_006717693.1:p.Ala1122Gly
XR_945604.3:n.4245C>G
XR_945605.3:n.4177C>G