Canonical Allele Identifier: CA508089772
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs2040124211
gnomAD v4: 19-49060932-C-T
MyVariant Identifiers: chr19:g.49564189C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060932C>T , CM000681.2:g.49060932C>T GRCh38
NC_000019.9:g.49564189C>T , CM000681.1:g.49564189C>T GRCh37
NC_000019.8:g.54256001C>T NCBI36
NG_016289.1:g.7936G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+823G>A ENSP00000470689.1:n.243+823G>A
XM_011527575.1:c.-180G>A XP_011525877.1:n.-180G>A
XR_001753693.1:n.879+232G>A
XR_001753694.1:n.880-123G>A
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