Canonical Allele Identifier: CA508089997
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060995-T-A
MyVariant Identifiers: chr19:g.49564252T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060995T>A , CM000681.2:g.49060995T>A GRCh38
NC_000019.9:g.49564252T>A , CM000681.1:g.49564252T>A GRCh37
NC_000019.8:g.54256064T>A NCBI36
NG_016289.1:g.7873A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+760A>T ENSP00000470689.1:n.243+760A>T
XR_001753693.1:n.879+169A>T
XR_001753694.1:n.879+169A>T
Search 100 bp 5'
Search 100 bp 3'