Canonical Allele Identifier: CA2340217029
Gene: NTF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060796C= , CM000681.2:g.49060796C= GRCh38
NC_000019.9:g.49564053C= , CM000681.1:g.49564053C= GRCh37
NC_000019.8:g.54255865C= NCBI36
NG_016289.1:g.8072G=

Transcript Alleles

HGVS Amino-acid change
ENST00000599795.5:c.243+959G= ENSP00000470689.1:n.243+959G=
XM_011527575.1:c.-44G= XP_011525877.1:n.-44G=
XR_001753693.1:n.879+368G=
XR_001753694.1:n.893G=