Canonical Allele Identifier: CA670630560

Gene: ABCC2

Linked Data

• dbSNP Id: rs1296114159
• gnomAD v3: 10-99830604-CT-C
• gnomAD v4: 10-99830604-CT-C
• MyVariant Identifiers: chr10:g.101590362del (hg19) ; chr10:g.99830605del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830605del , CM000672.2:g.99830605del	GRCh38
NC_000010.10:g.101590362del , CM000672.1:g.101590362del	GRCh37
NC_000010.9:g.101580352del	NCBI36
NG_011798.1:g.52900del
NG_011798.2:g.53008del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2748-111del MANE Select	ENSP00000497274.1:n.2748-111del
ENST00000370449.8:c.2748-111del	ENSP00000359478.4:n.2748-111del
NM_000392.4:c.2748-111del	NP_000383.1:n.2748-111del
XM_006717630.2:c.2052-111del	XP_006717693.1:n.2052-111del
XM_011539291.1:c.2747+172del	XP_011537593.1:n.2747+172del
XR_945604.1:n.2937-111del
XR_945605.1:n.2939-111del
NM_000392.5:c.2748-111del MANE Select	NP_000383.2:n.2748-111del
XM_006717630.3:c.2052-111del	XP_006717693.1:n.2052-111del
XM_011539291.3:c.2747+172del	XP_011537593.1:n.2747+172del
XR_945604.3:n.2991-111del
XR_945605.3:n.2991-111del