Canonical Allele Identifier: CA508088898
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060660-T-A
MyVariant Identifiers: chr19:g.49563917T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060660T>A , CM000681.2:g.49060660T>A GRCh38
NC_000019.9:g.49563917T>A , CM000681.1:g.49563917T>A GRCh37
NC_000019.8:g.54255729T>A NCBI36
NG_016289.1:g.8208A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+1095A>T ENSP00000470689.1:n.243+1095A>T
XM_011527575.1:c.40+53A>T XP_011525877.1:n.40+53A>T
XR_001753693.1:n.879+504A>T
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