Canonical Allele Identifier: CA378128233

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605474G>T (hg19) ; chr10:g.99845717G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845717G>T , CM000672.2:g.99845717G>T	GRCh38
NC_000010.10:g.101605474G>T , CM000672.1:g.101605474G>T	GRCh37
NC_000010.9:g.101595464G>T	NCBI36
NG_011798.1:g.68012G>T
NG_011798.2:g.68120G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4081G>T MANE Select	ENSP00000497274.1:p.Asp1361Tyr
ENST00000649459.1:n.429G>T
ENST00000370449.8:c.4081G>T	ENSP00000359478.4:p.Asp1361Tyr
NM_000392.4:c.4081G>T	NP_000383.1:p.Asp1361Tyr
XM_006717630.2:c.3385G>T	XP_006717693.1:p.Asp1129Tyr
XR_945604.1:n.4211G>T
XR_945605.1:n.4145G>T
NM_000392.5:c.4081G>T MANE Select	NP_000383.2:p.Asp1361Tyr
XM_006717630.3:c.3385G>T	XP_006717693.1:p.Asp1129Tyr
XR_945604.3:n.4265G>T
XR_945605.3:n.4197G>T