Canonical Allele Identifier: CA931721726

Gene: ABCC2

Linked Data

• dbSNP Id: rs2038983408
• gnomAD v3: 10-99844160-CT-C
• gnomAD v4: 10-99844160-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844163del , CM000672.2:g.99844163del	GRCh38
NC_000010.10:g.101603920del , CM000672.1:g.101603920del	GRCh37
NC_000010.9:g.101593910del	NCBI36
NG_011798.1:g.66458del
NG_011798.2:g.66566del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.3844-159del MANE Select	ENSP00000497274.1:n.3844-159del
ENST00000649459.1:n.192-159del
ENST00000370449.8:c.3844-159del	ENSP00000359478.4:n.3844-159del
NM_000392.4:c.3844-159del	NP_000383.1:n.3844-159del
XM_006717630.2:c.3148-159del	XP_006717693.1:n.3148-159del
XR_945604.1:n.4033-159del
XR_945605.1:n.3908-159del
NM_000392.5:c.3844-159del MANE Select	NP_000383.2:n.3844-159del
XM_006717630.3:c.3148-159del	XP_006717693.1:n.3148-159del
XR_945604.3:n.4087-159del
XR_945605.3:n.3960-159del