Canonical Allele Identifier: CA2610496161

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99830196-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99830199del , CM000672.2:g.99830199del	GRCh38
NC_000010.10:g.101589956del , CM000672.1:g.101589956del	GRCh37
NC_000010.9:g.101579946del	NCBI36
NG_011798.1:g.52494del
NG_011798.2:g.52602del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647814.1:c.2621-108del MANE Select	ENSP00000497274.1:n.2621-108del
ENST00000370449.8:c.2621-108del	ENSP00000359478.4:n.2621-108del
NM_000392.4:c.2621-108del	NP_000383.1:n.2621-108del
XM_006717630.2:c.1925-108del	XP_006717693.1:n.1925-108del
XM_006717631.2:c.*48-108del	XP_006717694.1:n.*48-108del
XM_011539291.1:c.2621-108del	XP_011537593.1:n.2621-108del
XR_945604.1:n.2810-108del
XR_945605.1:n.2812-108del
NM_000392.5:c.2621-108del MANE Select	NP_000383.2:n.2621-108del
XM_006717630.3:c.1925-108del	XP_006717693.1:n.1925-108del
XM_006717631.4:c.*48-108del	XP_006717694.1:n.*48-108del
XM_011539291.3:c.2621-108del	XP_011537593.1:n.2621-108del
XR_945604.3:n.2864-108del
XR_945605.3:n.2864-108del