Canonical Allele Identifier: CA378127878

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845649-C-T
• MyVariant Identifiers: chr10:g.101605406C>T (hg19) ; chr10:g.99845649C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845649C>T , CM000672.2:g.99845649C>T	GRCh38
NC_000010.10:g.101605406C>T , CM000672.1:g.101605406C>T	GRCh37
NC_000010.9:g.101595396C>T	NCBI36
NG_011798.1:g.67944C>T
NG_011798.2:g.68052C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4013C>T MANE Select	ENSP00000497274.1:p.Ala1338Val
ENST00000649459.1:n.361C>T
ENST00000370449.8:c.4013C>T	ENSP00000359478.4:p.Ala1338Val
NM_000392.4:c.4013C>T	NP_000383.1:p.Ala1338Val
XM_006717630.2:c.3317C>T	XP_006717693.1:p.Ala1106Val
XR_945604.1:n.4177-34C>T
XR_945605.1:n.4077C>T
NM_000392.5:c.4013C>T MANE Select	NP_000383.2:p.Ala1338Val
XM_006717630.3:c.3317C>T	XP_006717693.1:p.Ala1106Val
XR_945604.3:n.4231-34C>T
XR_945605.3:n.4129C>T