Canonical Allele Identifier: CA471135620

Gene: ABCC2

Linked Data

• dbSNP Id: rs1590192961
• MyVariant Identifiers: chr10:g.101605458T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845701T>G , CM000672.2:g.99845701T>G	GRCh38
NC_000010.10:g.101605458T>G , CM000672.1:g.101605458T>G	GRCh37
NC_000010.9:g.101595448T>G	NCBI36
NG_011798.1:g.67996T>G
NG_011798.2:g.68104T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.4065T>G MANE Select	ENSP00000497274.1:p.Gly1355=
ENST00000649459.1:n.413T>G
ENST00000370449.8:c.4065T>G	ENSP00000359478.4:p.Gly1355=
NM_000392.4:c.4065T>G	NP_000383.1:p.Gly1355=
XM_006717630.2:c.3369T>G	XP_006717693.1:p.Gly1123=
XR_945604.1:n.4195T>G
XR_945605.1:n.4129T>G
NM_000392.5:c.4065T>G MANE Select	NP_000383.2:p.Gly1355=
XM_006717630.3:c.3369T>G	XP_006717693.1:p.Gly1123=
XR_945604.3:n.4249T>G
XR_945605.3:n.4181T>G