Canonical Allele Identifier: CA2340217079
Gene: NTF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060946T= , CM000681.2:g.49060946T= GRCh38
NC_000019.9:g.49564203T= , CM000681.1:g.49564203T= GRCh37
NC_000019.8:g.54256015T= NCBI36
NG_016289.1:g.7922A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+809A= ENSP00000470689.1:n.243+809A=
XM_011527575.1:c.-194A= XP_011525877.1:n.-194A=
XR_001753693.1:n.879+218A=
XR_001753694.1:n.880-137A=