Canonical Allele Identifier: CA214099405
Gene: VTI1A HGNC NCBI

Linked Data

dbSNP Id: rs910544504
gnomAD v2: 10-114708491-C-T
gnomAD v3: 10-112948732-C-T
gnomAD v4: 10-112948732-C-T
MyVariant Identifiers: chr10:g.114708491C>T (hg19) chr10:g.112948732C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112948732C>T , CM000672.2:g.112948732C>T GRCh38
NC_000010.10:g.114708491C>T , CM000672.1:g.114708491C>T GRCh37
NC_000010.9:g.114698481C>T NCBI36
NG_012631.1:g.3483C>T

Transcript Alleles

HGVS Amino-acid Change
XR_002956958.1:n.4768C>T
Search 100 bp 5'
Search 100 bp 3'