Canonical Allele Identifier: CA1931495670

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038809483

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99835723del , CM000672.2:g.99835723del	GRCh38
NC_000010.10:g.101595480del , CM000672.1:g.101595480del	GRCh37
NC_000010.9:g.101585470del	NCBI36
NG_011798.1:g.58018del
NG_011798.2:g.58126del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3415-368del MANE Select	ENSP00000497274.1:n.3415-368del
ENST00000370449.8:c.3415-368del	ENSP00000359478.4:n.3415-368del
NM_000392.4:c.3415-368del	NP_000383.1:n.3415-368del
XM_006717630.2:c.2719-368del	XP_006717693.1:n.2719-368del
XR_945604.1:n.3604-368del
XR_945605.1:n.3606-368del
NM_000392.5:c.3415-368del MANE Select	NP_000383.2:n.3415-368del
XM_006717630.3:c.2719-368del	XP_006717693.1:n.2719-368del
XR_945604.3:n.3658-368del
XR_945605.3:n.3658-368del