Canonical Allele Identifier: CA378120324

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101590070A>T (hg19) ; chr10:g.99830313A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830313A>T , CM000672.2:g.99830313A>T	GRCh38
NC_000010.10:g.101590070A>T , CM000672.1:g.101590070A>T	GRCh37
NC_000010.9:g.101580060A>T	NCBI36
NG_011798.1:g.52608A>T
NG_011798.2:g.52716A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2627A>T MANE Select	ENSP00000497274.1:p.Asp876Val
ENST00000370449.8:c.2627A>T	ENSP00000359478.4:p.Asp876Val
NM_000392.4:c.2627A>T	NP_000383.1:p.Asp876Val
XM_006717630.2:c.1931A>T	XP_006717693.1:p.Asp644Val
XM_006717631.2:c.*54A>T	XP_006717694.1:n.*54A>T
XM_011539291.1:c.2627A>T	XP_011537593.1:p.Asp876Val
XR_945604.1:n.2816A>T
XR_945605.1:n.2818A>T
NM_000392.5:c.2627A>T MANE Select	NP_000383.2:p.Asp876Val
XM_006717630.3:c.1931A>T	XP_006717693.1:p.Asp644Val
XM_006717631.4:c.*54A>T	XP_006717694.1:n.*54A>T
XM_011539291.3:c.2627A>T	XP_011537593.1:p.Asp876Val
XR_945604.3:n.2870A>T
XR_945605.3:n.2870A>T