Canonical Allele Identifier: CA378127761

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605381A>G (hg19) ; chr10:g.99845624A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845624A>G , CM000672.2:g.99845624A>G	GRCh38
NC_000010.10:g.101605381A>G , CM000672.1:g.101605381A>G	GRCh37
NC_000010.9:g.101595371A>G	NCBI36
NG_011798.1:g.67919A>G
NG_011798.2:g.68027A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3988A>G MANE Select	ENSP00000497274.1:p.Ile1330Val
ENST00000649459.1:n.336A>G
ENST00000370449.8:c.3988A>G	ENSP00000359478.4:p.Ile1330Val
NM_000392.4:c.3988A>G	NP_000383.1:p.Ile1330Val
XM_006717630.2:c.3292A>G	XP_006717693.1:p.Ile1098Val
XR_945604.1:n.4177-59A>G
XR_945605.1:n.4052A>G
NM_000392.5:c.3988A>G MANE Select	NP_000383.2:p.Ile1330Val
XM_006717630.3:c.3292A>G	XP_006717693.1:p.Ile1098Val
XR_945604.3:n.4231-59A>G
XR_945605.3:n.4104A>G