Canonical Allele Identifier: CA2340217032
Gene: NTF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060811T= , CM000681.2:g.49060811T= GRCh38
NC_000019.9:g.49564068T= , CM000681.1:g.49564068T= GRCh37
NC_000019.8:g.54255880T= NCBI36
NG_016289.1:g.8057A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+944A= ENSP00000470689.1:n.243+944A=
XM_011527575.1:c.-59A= XP_011525877.1:n.-59A=
XR_001753693.1:n.879+353A=
XR_001753694.1:n.880-2A=