Canonical Allele Identifier: CA508089891
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060965-C-A
MyVariant Identifiers: chr19:g.49564222C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060965C>A , CM000681.2:g.49060965C>A GRCh38
NC_000019.9:g.49564222C>A , CM000681.1:g.49564222C>A GRCh37
NC_000019.8:g.54256034C>A NCBI36
NG_016289.1:g.7903G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+790G>T ENSP00000470689.1:n.243+790G>T
XM_011527575.1:c.-213G>T XP_011525877.1:n.-213G>T
XR_001753693.1:n.879+199G>T
XR_001753694.1:n.880-156G>T
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