Canonical Allele Identifier: CA471135376

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99845635-G-C
• MyVariant Identifiers: chr10:g.101605392G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99845635G>C , CM000672.2:g.99845635G>C	GRCh38
NC_000010.10:g.101605392G>C , CM000672.1:g.101605392G>C	GRCh37
NC_000010.9:g.101595382G>C	NCBI36
NG_011798.1:g.67930G>C
NG_011798.2:g.68038G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3999G>C MANE Select	ENSP00000497274.1:p.Val1333=
ENST00000649459.1:n.347G>C
ENST00000370449.8:c.3999G>C	ENSP00000359478.4:p.Val1333=
NM_000392.4:c.3999G>C	NP_000383.1:p.Val1333=
XM_006717630.2:c.3303G>C	XP_006717693.1:p.Val1101=
XR_945604.1:n.4177-48G>C
XR_945605.1:n.4063G>C
NM_000392.5:c.3999G>C MANE Select	NP_000383.2:p.Val1333=
XM_006717630.3:c.3303G>C	XP_006717693.1:p.Val1101=
XR_945604.3:n.4231-48G>C
XR_945605.3:n.4115G>C