Canonical Allele Identifier: CA14673775
Gene: VSTM2B-DT HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_040029.1:n.410-4234T>C
NR_040029.2:n.408-4234T>C
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Search 100 bp 3'