Canonical Allele Identifier: CA309446079
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs937223346
gnomAD v2: 19-49564248-C-T
gnomAD v3: 19-49060991-C-T
gnomAD v4: 19-49060991-C-T
MyVariant Identifiers: chr19:g.49564248C>T (hg19) chr19:g.49060991C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060991C>T , CM000681.2:g.49060991C>T GRCh38
NC_000019.9:g.49564248C>T , CM000681.1:g.49564248C>T GRCh37
NC_000019.8:g.54256060C>T NCBI36
NG_016289.1:g.7877G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+764G>A ENSP00000470689.1:n.243+764G>A
XR_001753693.1:n.879+173G>A
XR_001753694.1:n.879+173G>A
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