Canonical Allele Identifier: CA214099413
Gene: VTI1A HGNC NCBI

Linked Data

dbSNP Id: rs1047333326
MyVariant Identifiers: chr10:g.114708571A>C (hg19) chr10:g.112948812A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112948812A>C , CM000672.2:g.112948812A>C GRCh38
NC_000010.10:g.114708571A>C , CM000672.1:g.114708571A>C GRCh37
NC_000010.9:g.114698561A>C NCBI36
NG_012631.1:g.3563A>C

Transcript Alleles

HGVS Amino-acid change
XR_002956958.1:n.4848A>C
Search 100 bp 5'
Search 100 bp 3'