Canonical Allele Identifier: CA670630519

Gene: ABCC2

Linked Data

• dbSNP Id: rs1168339026
• gnomAD v3: 10-99830544-G-C
• gnomAD v4: 10-99830544-G-C
• MyVariant Identifiers: chr10:g.101590301G>C (hg19) ; chr10:g.99830544G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830544G>C , CM000672.2:g.99830544G>C	GRCh38
NC_000010.10:g.101590301G>C , CM000672.1:g.101590301G>C	GRCh37
NC_000010.9:g.101580291G>C	NCBI36
NG_011798.1:g.52839G>C
NG_011798.2:g.52947G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+111G>C MANE Select	ENSP00000497274.1:n.2747+111G>C
ENST00000370449.8:c.2747+111G>C	ENSP00000359478.4:n.2747+111G>C
NM_000392.4:c.2747+111G>C	NP_000383.1:n.2747+111G>C
XM_006717630.2:c.2051+111G>C	XP_006717693.1:n.2051+111G>C
XM_011539291.1:c.2747+111G>C	XP_011537593.1:n.2747+111G>C
XR_945604.1:n.2936+111G>C
XR_945605.1:n.2938+111G>C
NM_000392.5:c.2747+111G>C MANE Select	NP_000383.2:n.2747+111G>C
XM_006717630.3:c.2051+111G>C	XP_006717693.1:n.2051+111G>C
XM_011539291.3:c.2747+111G>C	XP_011537593.1:n.2747+111G>C
XR_945604.3:n.2990+111G>C
XR_945605.3:n.2990+111G>C