Canonical Allele Identifier: CA432779014
Gene: VENTXP7 HGNC NCBI

Linked Data

gnomAD v4: 3-21405746-T-C
MyVariant Identifiers: chr3:g.21447238T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21405746T>C , CM000665.2:g.21405746T>C GRCh38
NC_000003.11:g.21447238T>C , CM000665.1:g.21447238T>C GRCh37
NC_000003.10:g.21422242T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475503.1:n.10T>C
NR_002311.1:n.21T>C