Canonical Allele Identifier: CA1863320626
Gene: LINC01508 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.90419249G= , CM000671.2:g.90419249G= GRCh38
NC_000009.11:g.93181531G= , CM000671.1:g.93181531G= GRCh37
NC_000009.10:g.92221351G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109795.1:n.59+14182C=