Canonical Allele Identifier: CA13148516

Gene: APBB1IP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26445658C>T , CM000672.2:g.26445658C>T	GRCh38
NC_000010.10:g.26734587C>T , CM000672.1:g.26734587C>T	GRCh37
NC_000010.9:g.26774593C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376236.9:c.-1+6805C>T MANE Select	ENSP00000365411.4:n.-1+6805C>T
ENST00000356785.4:c.-1+6805C>T	ENSP00000349237.4:n.-1+6805C>T
ENST00000376236.8:c.-1+6805C>T	ENSP00000365411.4:n.-1+6805C>T
NM_019043.3:c.-1+6805C>T	NP_061916.3:n.-1+6805C>T
XM_011519514.1:c.-1+6805C>T	XP_011517816.1:n.-1+6805C>T
XM_011519514.2:c.-1+6805C>T	XP_011517816.1:n.-1+6805C>T
NM_019043.4:c.-1+6805C>T MANE Select	NP_061916.3:n.-1+6805C>T