Canonical Allele Identifier: CA378126639

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101604082C>G (hg19) ; chr10:g.99844325C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844325C>G , CM000672.2:g.99844325C>G	GRCh38
NC_000010.10:g.101604082C>G , CM000672.1:g.101604082C>G	GRCh37
NC_000010.9:g.101594072C>G	NCBI36
NG_011798.1:g.66620C>G
NG_011798.2:g.66728C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3847C>G MANE Select	ENSP00000497274.1:p.Pro1283Ala
ENST00000649459.1:n.195C>G
ENST00000370449.8:c.3847C>G	ENSP00000359478.4:p.Pro1283Ala
NM_000392.4:c.3847C>G	NP_000383.1:p.Pro1283Ala
XM_006717630.2:c.3151C>G	XP_006717693.1:p.Pro1051Ala
XR_945604.1:n.4036C>G
XR_945605.1:n.3911C>G
NM_000392.5:c.3847C>G MANE Select	NP_000383.2:p.Pro1283Ala
XM_006717630.3:c.3151C>G	XP_006717693.1:p.Pro1051Ala
XR_945604.3:n.4090C>G
XR_945605.3:n.3963C>G