Canonical Allele Identifier: CA432779025
Gene: VENTXP7 HGNC NCBI

Linked Data

gnomAD v4: 3-21405750-C-A
MyVariant Identifiers: chr3:g.21447242C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21405750C>A , CM000665.2:g.21405750C>A GRCh38
NC_000003.11:g.21447242C>A , CM000665.1:g.21447242C>A GRCh37
NC_000003.10:g.21422246C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475503.1:n.14C>A
NR_002311.1:n.25C>A