Canonical Allele Identifier: CA485061545

Gene: LINC00452

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113919624A>T , CM000675.2:g.113919624A>T	GRCh38
NC_000013.10:g.114622597A>T , CM000675.1:g.114622597A>T	GRCh37
NC_000013.9:g.113491346T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001278674.1:c.503A>T	NP_001265603.1:p.Asn168Ile
XM_011534843.1:c.701A>T	XP_011533145.1:p.Asn234Ile
XR_941409.1:n.875A>T
XR_941410.1:n.875A>T
XR_941411.1:n.875A>T
XR_941412.1:n.875A>T
XR_941413.1:n.872A>T
XR_941414.1:n.2055A>T
XR_941415.1:n.945A>T
XR_941416.1:n.2016A>T
XR_941417.1:n.1954A>T
XR_941418.1:n.1949A>T
XR_941419.1:n.1810A>T
XR_941420.1:n.1795A>T
XR_941421.1:n.651A>T
XR_001749638.1:n.651A>T
XR_001749639.1:n.651A>T
XR_941421.2:n.651A>T
NR_164112.1:n.1111A>T