Canonical Allele Identifier: CA2340217086
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs2040124617

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060964_49060966del , CM000681.2:g.49060964_49060966del GRCh38
NC_000019.9:g.49564221_49564223del , CM000681.1:g.49564221_49564223del GRCh37
NC_000019.8:g.54256033_54256035del NCBI36
NG_016289.1:g.7909_7911del

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+796_243+798del ENSP00000470689.1:n.243+796_243+798del
XR_001753693.1:n.879+205_879+207del
XR_001753694.1:n.880-150_880-148del