Canonical Allele Identifier: CA2574638300

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99817271G>T , CM000672.2:g.99817271G>T	GRCh38
NC_000010.10:g.101577028G>T , CM000672.1:g.101577028G>T	GRCh37
NC_000010.9:g.101567018G>T	NCBI36
NG_011798.1:g.39566G>T
NG_011798.2:g.39674G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2095-37G>T MANE Select	ENSP00000497274.1:n.2095-37G>T
ENST00000370449.8:c.2095-37G>T	ENSP00000359478.4:n.2095-37G>T
NM_000392.4:c.2095-37G>T	NP_000383.1:n.2095-37G>T
XM_006717630.2:c.1399-37G>T	XP_006717693.1:n.1399-37G>T
XM_006717631.2:c.2095-37G>T	XP_006717694.1:n.2095-37G>T
XM_011539291.1:c.2095-37G>T	XP_011537593.1:n.2095-37G>T
XR_945604.1:n.2284-37G>T
XR_945605.1:n.2286-37G>T
NM_000392.5:c.2095-37G>T MANE Select	NP_000383.2:n.2095-37G>T
XM_006717630.3:c.1399-37G>T	XP_006717693.1:n.1399-37G>T
XM_006717631.4:c.2095-37G>T	XP_006717694.1:n.2095-37G>T
XM_011539291.3:c.2095-37G>T	XP_011537593.1:n.2095-37G>T
XM_017015675.2:c.2095-37G>T	XP_016871164.1:n.2095-37G>T
XR_945604.3:n.2338-37G>T
XR_945605.3:n.2338-37G>T