Canonical Allele Identifier: CA5643552

Gene: ABCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830363G>A , CM000672.2:g.99830363G>A	GRCh38
NC_000010.10:g.101590120G>A , CM000672.1:g.101590120G>A	GRCh37
NC_000010.9:g.101580110G>A	NCBI36
NG_011798.1:g.52658G>A
NG_011798.2:g.52766G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000392.5:c.2677G>A MANE Select	NP_000383.2:p.Glu893Lys
ENST00000647814.1:c.2677G>A MANE Select	ENSP00000497274.1:p.Glu893Lys
NM_000392.4:c.2677G>A	NP_000383.1:p.Glu893Lys
ENST00000370449.8:c.2677G>A	ENSP00000359478.4:p.Glu893Lys
XM_006717630.2:c.1981G>A	XP_006717693.1:p.Glu661Lys
XM_006717630.3:c.1981G>A	XP_006717693.1:p.Glu661Lys
XM_006717631.2:c.*104G>A	XP_006717694.1:n.*104G>A
XM_006717631.4:c.*104G>A	XP_006717694.1:n.*104G>A
XM_011539291.1:c.2677G>A	XP_011537593.1:p.Glu893Lys
XM_011539291.3:c.2677G>A	XP_011537593.1:p.Glu893Lys
XR_945604.1:n.2866G>A
XR_945604.3:n.2920G>A
XR_945605.1:n.2868G>A
XR_945605.3:n.2920G>A