Canonical Allele Identifier: CA2340217069
Gene: NTF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060913G= , CM000681.2:g.49060913G= GRCh38
NC_000019.9:g.49564170G= , CM000681.1:g.49564170G= GRCh37
NC_000019.8:g.54255982G= NCBI36
NG_016289.1:g.7955C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+842C= ENSP00000470689.1:n.243+842C=
XM_011527575.1:c.-161C= XP_011525877.1:n.-161C=
XR_001753693.1:n.879+251C=
XR_001753694.1:n.880-104C=