Canonical Allele Identifier: CA432779039
Gene: VENTXP7 HGNC NCBI

Linked Data

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

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

Transcript Alleles

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