Canonical Allele Identifier: CA508089536
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564119T>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060862T>A , CM000681.2:g.49060862T>A GRCh38
NC_000019.9:g.49564119T>A , CM000681.1:g.49564119T>A GRCh37
NC_000019.8:g.54255931T>A NCBI36
NG_016289.1:g.8006A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+893A>T ENSP00000470689.1:n.243+893A>T
XM_011527575.1:c.-110A>T XP_011525877.1:n.-110A>T
XR_001753693.1:n.879+302A>T
XR_001753694.1:n.880-53A>T
Search 100 bp 5'
Search 100 bp 3'