Canonical Allele Identifier: CA378116592

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101577131T>A (hg19) ; chr10:g.99817374T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817374T>A , CM000672.2:g.99817374T>A	GRCh38
NC_000010.10:g.101577131T>A , CM000672.1:g.101577131T>A	GRCh37
NC_000010.9:g.101567121T>A	NCBI36
NG_011798.1:g.39669T>A
NG_011798.2:g.39777T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2161T>A MANE Select	ENSP00000497274.1:p.Phe721Ile
ENST00000370449.8:c.2161T>A	ENSP00000359478.4:p.Phe721Ile
NM_000392.4:c.2161T>A	NP_000383.1:p.Phe721Ile
XM_006717630.2:c.1465T>A	XP_006717693.1:p.Phe489Ile
XM_006717631.2:c.2161T>A	XP_006717694.1:p.Phe721Ile
XM_011539291.1:c.2161T>A	XP_011537593.1:p.Phe721Ile
XR_945604.1:n.2350T>A
XR_945605.1:n.2352T>A
NM_000392.5:c.2161T>A MANE Select	NP_000383.2:p.Phe721Ile
XM_006717630.3:c.1465T>A	XP_006717693.1:p.Phe489Ile
XM_006717631.4:c.2161T>A	XP_006717694.1:p.Phe721Ile
XM_011539291.3:c.2161T>A	XP_011537593.1:p.Phe721Ile
XM_017015675.2:c.2161T>A	XP_016871164.1:p.Phe721Ile
XR_945604.3:n.2404T>A
XR_945605.3:n.2404T>A