Canonical Allele Identifier: CA214099414

Gene: VTI1A

Linked Data

• dbSNP Id: rs536353863
• gnomAD v3: 10-112948817-T-C
• gnomAD v4: 10-112948817-T-C
• MyVariant Identifiers: chr10:g.114708576T>C (hg19) ; chr10:g.112948817T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.112948817T>C , CM000672.2:g.112948817T>C	GRCh38
NC_000010.10:g.114708576T>C , CM000672.1:g.114708576T>C	GRCh37
NC_000010.9:g.114698566T>C	NCBI36
NG_012631.1:g.3568T>C

Transcript Alleles

HGVS	Amino-acid change
XR_002956958.1:n.4853T>C