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

Linked Data

dbSNP Id: rs10425935
gnomAD v2: 19-29908107-A-G
gnomAD v3: 19-29417200-A-G
gnomAD v4: 19-29417200-A-G
MyVariant Identifiers: chr19:g.29908107A>G (hg19) chr19:g.29417200A>G (hg38)
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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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