Canonical Allele Identifier: CA508089425
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564083C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060826C>T , CM000681.2:g.49060826C>T GRCh38
NC_000019.9:g.49564083C>T , CM000681.1:g.49564083C>T GRCh37
NC_000019.8:g.54255895C>T NCBI36
NG_016289.1:g.8042G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+929G>A ENSP00000470689.1:n.243+929G>A
XM_011527575.1:c.-74G>A XP_011525877.1:n.-74G>A
XR_001753693.1:n.879+338G>A
XR_001753694.1:n.880-17G>A
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