Canonical Allele Identifier: CA1931489467

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038720320
• gnomAD v4: 10-99830508-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830512del , CM000672.2:g.99830512del	GRCh38
NC_000010.10:g.101590269del , CM000672.1:g.101590269del	GRCh37
NC_000010.9:g.101580259del	NCBI36
NG_011798.1:g.52807del
NG_011798.2:g.52915del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2747+79del MANE Select	ENSP00000497274.1:n.2747+79del
ENST00000370449.8:c.2747+79del	ENSP00000359478.4:n.2747+79del
NM_000392.4:c.2747+79del	NP_000383.1:n.2747+79del
XM_006717630.2:c.2051+79del	XP_006717693.1:n.2051+79del
XM_011539291.1:c.2747+79del	XP_011537593.1:n.2747+79del
XR_945604.1:n.2936+79del
XR_945605.1:n.2938+79del
NM_000392.5:c.2747+79del MANE Select	NP_000383.2:n.2747+79del
XM_006717630.3:c.2051+79del	XP_006717693.1:n.2051+79del
XM_011539291.3:c.2747+79del	XP_011537593.1:n.2747+79del
XR_945604.3:n.2990+79del
XR_945605.3:n.2990+79del