Canonical Allele Identifier: CA378120318

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101590068T>G (hg19) ; chr10:g.99830311T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830311T>G , CM000672.2:g.99830311T>G	GRCh38
NC_000010.10:g.101590068T>G , CM000672.1:g.101590068T>G	GRCh37
NC_000010.9:g.101580058T>G	NCBI36
NG_011798.1:g.52606T>G
NG_011798.2:g.52714T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2625T>G MANE Select	ENSP00000497274.1:p.His875Gln
ENST00000370449.8:c.2625T>G	ENSP00000359478.4:p.His875Gln
NM_000392.4:c.2625T>G	NP_000383.1:p.His875Gln
XM_006717630.2:c.1929T>G	XP_006717693.1:p.His643Gln
XM_006717631.2:c.*52T>G	XP_006717694.1:n.*52T>G
XM_011539291.1:c.2625T>G	XP_011537593.1:p.His875Gln
XR_945604.1:n.2814T>G
XR_945605.1:n.2816T>G
NM_000392.5:c.2625T>G MANE Select	NP_000383.2:p.His875Gln
XM_006717630.3:c.1929T>G	XP_006717693.1:p.His643Gln
XM_006717631.4:c.*52T>G	XP_006717694.1:n.*52T>G
XM_011539291.3:c.2625T>G	XP_011537593.1:p.His875Gln
XR_945604.3:n.2868T>G
XR_945605.3:n.2868T>G