Canonical Allele Identifier: CA508089381
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs2040122145
gnomAD v3: 19-49060812-C-A
gnomAD v4: 19-49060812-C-A
MyVariant Identifiers: chr19:g.49564069C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060812C>A , CM000681.2:g.49060812C>A GRCh38
NC_000019.9:g.49564069C>A , CM000681.1:g.49564069C>A GRCh37
NC_000019.8:g.54255881C>A NCBI36
NG_016289.1:g.8056G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+943G>T ENSP00000470689.1:n.243+943G>T
XM_011527575.1:c.-60G>T XP_011525877.1:n.-60G>T
XR_001753693.1:n.879+352G>T
XR_001753694.1:n.880-3G>T
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