Canonical Allele Identifier: CA378128032

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605438A>T (hg19) ; chr10:g.99845681A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845681A>T , CM000672.2:g.99845681A>T	GRCh38
NC_000010.10:g.101605438A>T , CM000672.1:g.101605438A>T	GRCh37
NC_000010.9:g.101595428A>T	NCBI36
NG_011798.1:g.67976A>T
NG_011798.2:g.68084A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4045A>T MANE Select	ENSP00000497274.1:p.Arg1349Ter
ENST00000649459.1:n.393A>T
ENST00000370449.8:c.4045A>T	ENSP00000359478.4:p.Arg1349Ter
NM_000392.4:c.4045A>T	NP_000383.1:p.Arg1349Ter
XM_006717630.2:c.3349A>T	XP_006717693.1:p.Arg1117Ter
XR_945604.1:n.4177-2A>T
XR_945605.1:n.4109A>T
NM_000392.5:c.4045A>T MANE Select	NP_000383.2:p.Arg1349Ter
XM_006717630.3:c.3349A>T	XP_006717693.1:p.Arg1117Ter
XR_945604.3:n.4231-2A>T
XR_945605.3:n.4161A>T