Canonical Allele Identifier: CA2610497701

Gene: ABCC2

Linked Data

• gnomAD v4: 10-99844261-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844263del , CM000672.2:g.99844263del	GRCh38
NC_000010.10:g.101604020del , CM000672.1:g.101604020del	GRCh37
NC_000010.9:g.101594010del	NCBI36
NG_011798.1:g.66558del
NG_011798.2:g.66666del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3844-59del MANE Select	ENSP00000497274.1:n.3844-59del
ENST00000649459.1:n.192-59del
ENST00000370449.8:c.3844-59del	ENSP00000359478.4:n.3844-59del
NM_000392.4:c.3844-59del	NP_000383.1:n.3844-59del
XM_006717630.2:c.3148-59del	XP_006717693.1:n.3148-59del
XR_945604.1:n.4033-59del
XR_945605.1:n.3908-59del
NM_000392.5:c.3844-59del MANE Select	NP_000383.2:n.3844-59del
XM_006717630.3:c.3148-59del	XP_006717693.1:n.3148-59del
XR_945604.3:n.4087-59del
XR_945605.3:n.3960-59del