Canonical Allele Identifier: CA471131298

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101590065C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830308C>A , CM000672.2:g.99830308C>A	GRCh38
NC_000010.10:g.101590065C>A , CM000672.1:g.101590065C>A	GRCh37
NC_000010.9:g.101580055C>A	NCBI36
NG_011798.1:g.52603C>A
NG_011798.2:g.52711C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.2622C>A MANE Select	ENSP00000497274.1:p.Val874=
ENST00000370449.8:c.2622C>A	ENSP00000359478.4:p.Val874=
NM_000392.4:c.2622C>A	NP_000383.1:p.Val874=
XM_006717630.2:c.1926C>A	XP_006717693.1:p.Val642=
XM_006717631.2:c.*49C>A	XP_006717694.1:n.*49C>A
XM_011539291.1:c.2622C>A	XP_011537593.1:p.Val874=
XR_945604.1:n.2811C>A
XR_945605.1:n.2813C>A
NM_000392.5:c.2622C>A MANE Select	NP_000383.2:p.Val874=
XM_006717630.3:c.1926C>A	XP_006717693.1:p.Val642=
XM_006717631.4:c.*49C>A	XP_006717694.1:n.*49C>A
XM_011539291.3:c.2622C>A	XP_011537593.1:p.Val874=
XR_945604.3:n.2865C>A
XR_945605.3:n.2865C>A