Canonical Allele Identifier: CA378127590

Gene: ABCC2

Linked Data

• dbSNP Id: rs1388985149
• gnomAD v2: 10-101604212-G-A
• gnomAD v4: 10-99844455-G-A
• MyVariant Identifiers: chr10:g.101604212G>A (hg19) ; chr10:g.99844455G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844455G>A , CM000672.2:g.99844455G>A	GRCh38
NC_000010.10:g.101604212G>A , CM000672.1:g.101604212G>A	GRCh37
NC_000010.9:g.101594202G>A	NCBI36
NG_011798.1:g.66750G>A
NG_011798.2:g.66858G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3977G>A MANE Select	ENSP00000497274.1:p.Ser1326Asn
ENST00000649459.1:n.325G>A
ENST00000370449.8:c.3977G>A	ENSP00000359478.4:p.Ser1326Asn
NM_000392.4:c.3977G>A	NP_000383.1:p.Ser1326Asn
XM_006717630.2:c.3281G>A	XP_006717693.1:p.Ser1094Asn
XR_945604.1:n.4166G>A
XR_945605.1:n.4041G>A
NM_000392.5:c.3977G>A MANE Select	NP_000383.2:p.Ser1326Asn
XM_006717630.3:c.3281G>A	XP_006717693.1:p.Ser1094Asn
XR_945604.3:n.4220G>A
XR_945605.3:n.4093G>A