Canonical Allele Identifier: CA508089935
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1217719057
gnomAD v4: 19-49060977-T-A
MyVariant Identifiers: chr19:g.49564234T>A (hg19) chr19:g.49060977T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060977T>A , CM000681.2:g.49060977T>A GRCh38
NC_000019.9:g.49564234T>A , CM000681.1:g.49564234T>A GRCh37
NC_000019.8:g.54256046T>A NCBI36
NG_016289.1:g.7891A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+778A>T ENSP00000470689.1:n.243+778A>T
XR_001753693.1:n.879+187A>T
XR_001753694.1:n.880-168A>T
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