Canonical Allele Identifier: CA1863620019
Gene: LINC02937 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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