Canonical Allele Identifier: CA1350383329
Gene: VENTXP7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21405752T= , CM000665.2:g.21405752T= GRCh38
NC_000003.11:g.21447244T= , CM000665.1:g.21447244T= GRCh37
NC_000003.10:g.21422248T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475503.1:n.16T=
NR_002311.1:n.27T=