Canonical Allele Identifier: CA1937131899
Gene: VTI1A HGNC NCBI

Linked Data

dbSNP Id: rs2030360766

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.112948824G>C , CM000672.2:g.112948824G>C GRCh38
NC_000010.10:g.114708583G>C , CM000672.1:g.114708583G>C GRCh37
NC_000010.9:g.114698573G>C NCBI36
NG_012631.1:g.3575G>C

Transcript Alleles

HGVS Amino-acid change
XR_002956958.1:n.4860G>C