Canonical Allele Identifier: CA14726528
Gene: VSTM2B-DT HGNC NCBI

Linked Data

dbSNP Id: rs892073

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.29421387G>T , CM000681.2:g.29421387G>T GRCh38
NC_000019.9:g.29912294G>T , CM000681.1:g.29912294G>T GRCh37
NC_000019.8:g.34604134G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040029.1:n.409+7344C>A
NR_040029.2:n.407+7344C>A