Canonical Allele Identifier: CA309446060
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs865815501
gnomAD v2: 19-49564156-C-T
gnomAD v3: 19-49060899-C-T
gnomAD v4: 19-49060899-C-T
MyVariant Identifiers: chr19:g.49564156C>T (hg19) chr19:g.49060899C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060899C>T , CM000681.2:g.49060899C>T GRCh38
NC_000019.9:g.49564156C>T , CM000681.1:g.49564156C>T GRCh37
NC_000019.8:g.54255968C>T NCBI36
NG_016289.1:g.7969G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+856G>A ENSP00000470689.1:n.243+856G>A
XM_011527575.1:c.-147G>A XP_011525877.1:n.-147G>A
XR_001753693.1:n.879+265G>A
XR_001753694.1:n.880-90G>A
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