Canonical Allele Identifier: CA2340216995
Gene: NTF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060694A= , CM000681.2:g.49060694A= GRCh38
NC_000019.9:g.49563951A= , CM000681.1:g.49563951A= GRCh37
NC_000019.8:g.54255763A= NCBI36
NG_016289.1:g.8174T=

Transcript Alleles

HGVS Amino-acid change
ENST00000599795.5:c.243+1061T= ENSP00000470689.1:n.243+1061T=
XM_011527575.1:c.40+19T= XP_011525877.1:n.40+19T=
XR_001753693.1:n.879+470T=