Canonical Allele Identifier: CA1863620020
Gene: LINC02937 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91090533G>A , CM000671.2:g.91090533G>A GRCh38
NC_000009.11:g.93852815G>A , CM000671.1:g.93852815G>A GRCh37
NC_000009.10:g.92892636G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746830.2:n.13193+7889C>T