Canonical Allele Identifier: CA2330770230
Gene: VSTM2B-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.29417200A= , CM000681.2:g.29417200A= GRCh38
NC_000019.9:g.29908107A= , CM000681.1:g.29908107A= GRCh37
NC_000019.8:g.34599947A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_040029.1:n.410-4234T=
NR_040029.2:n.408-4234T=