Canonical Allele Identifier: CA1140029882
Gene: LINC02238 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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