Canonical Allele Identifier: CA432779038
Gene: VENTXP7 HGNC NCBI

Linked Data

gnomAD v4: 3-21405754-C-G
MyVariant Identifiers: chr3:g.21447246C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21405754C>G , CM000665.2:g.21405754C>G GRCh38
NC_000003.11:g.21447246C>G , CM000665.1:g.21447246C>G GRCh37
NC_000003.10:g.21422250C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475503.1:n.18C>G
NR_002311.1:n.29C>G