Canonical Allele Identifier: CA2574637942

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99782745A>T , CM000672.2:g.99782745A>T	GRCh38
NC_000010.10:g.101542502A>T , CM000672.1:g.101542502A>T	GRCh37
NC_000010.9:g.101532492A>T	NCBI36
NG_011798.1:g.5040A>T
NG_011798.2:g.5148A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.-100A>T MANE Select	ENSP00000497274.1:n.-100A>T
ENST00000647836.1:n.106A>T
ENST00000648324.1:c.-100A>T	ENSP00000497248.1:n.-100A>T
ENST00000648689.1:c.-100A>T	ENSP00000496972.1:n.-100A>T
ENST00000649932.1:c.-100A>T	ENSP00000498120.1:n.-100A>T
ENST00000370449.8:c.-100A>T	ENSP00000359478.4:n.-100A>T
NM_000392.4:c.-100A>T	NP_000383.1:n.-100A>T
XM_006717631.2:c.-100A>T	XP_006717694.1:n.-100A>T
XM_011539291.1:c.-100A>T	XP_011537593.1:n.-100A>T
XR_945604.1:n.90A>T
XR_945605.1:n.92A>T
NM_000392.5:c.-100A>T MANE Select	NP_000383.2:n.-100A>T
XM_006717631.4:c.-100A>T	XP_006717694.1:n.-100A>T
XM_011539291.3:c.-100A>T	XP_011537593.1:n.-100A>T
XM_017015675.2:c.-100A>T	XP_016871164.1:n.-100A>T
XR_945604.3:n.144A>T
XR_945605.3:n.144A>T