Canonical Allele Identifier: CA378127813

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101605394G>C (hg19) ; chr10:g.99845637G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845637G>C , CM000672.2:g.99845637G>C	GRCh38
NC_000010.10:g.101605394G>C , CM000672.1:g.101605394G>C	GRCh37
NC_000010.9:g.101595384G>C	NCBI36
NG_011798.1:g.67932G>C
NG_011798.2:g.68040G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.4001G>C MANE Select	ENSP00000497274.1:p.Gly1334Ala
ENST00000649459.1:n.349G>C
ENST00000370449.8:c.4001G>C	ENSP00000359478.4:p.Gly1334Ala
NM_000392.4:c.4001G>C	NP_000383.1:p.Gly1334Ala
XM_006717630.2:c.3305G>C	XP_006717693.1:p.Gly1102Ala
XR_945604.1:n.4177-46G>C
XR_945605.1:n.4065G>C
NM_000392.5:c.4001G>C MANE Select	NP_000383.2:p.Gly1334Ala
XM_006717630.3:c.3305G>C	XP_006717693.1:p.Gly1102Ala
XR_945604.3:n.4231-46G>C
XR_945605.3:n.4117G>C