Canonical Allele Identifier: CA378126722

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101604119C>A (hg19) ; chr10:g.99844362C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844362C>A , CM000672.2:g.99844362C>A	GRCh38
NC_000010.10:g.101604119C>A , CM000672.1:g.101604119C>A	GRCh37
NC_000010.9:g.101594109C>A	NCBI36
NG_011798.1:g.66657C>A
NG_011798.2:g.66765C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3884C>A MANE Select	ENSP00000497274.1:p.Pro1295His
ENST00000649459.1:n.232C>A
ENST00000370449.8:c.3884C>A	ENSP00000359478.4:p.Pro1295His
NM_000392.4:c.3884C>A	NP_000383.1:p.Pro1295His
XM_006717630.2:c.3188C>A	XP_006717693.1:p.Pro1063His
XR_945604.1:n.4073C>A
XR_945605.1:n.3948C>A
NM_000392.5:c.3884C>A MANE Select	NP_000383.2:p.Pro1295His
XM_006717630.3:c.3188C>A	XP_006717693.1:p.Pro1063His
XR_945604.3:n.4127C>A
XR_945605.3:n.4000C>A