Canonical Allele Identifier: CA214099410
Gene: VTI1A HGNC NCBI

Linked Data

dbSNP Id: rs923322155
gnomAD v2: 10-114708556-G-C
gnomAD v3: 10-112948797-G-C
gnomAD v4: 10-112948797-G-C
MyVariant Identifiers: chr10:g.114708556G>C (hg19) chr10:g.112948797G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112948797G>C , CM000672.2:g.112948797G>C GRCh38
NC_000010.10:g.114708556G>C , CM000672.1:g.114708556G>C GRCh37
NC_000010.9:g.114698546G>C NCBI36
NG_012631.1:g.3548G>C

Transcript Alleles

HGVS Amino-acid change
XR_002956958.1:n.4833G>C
Search 100 bp 5'
Search 100 bp 3'