Canonical Allele Identifier: CA738682790

Gene: LINC02238

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.73709607A>T , CM000663.2:g.73709607A>T	GRCh38
NC_000001.10:g.74175290A>T , CM000663.1:g.74175290A>T	GRCh37
NC_000001.9:g.73947878A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_146300.1:n.473+182A>T