Canonical Allele Identifier: CA508089089
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49563978A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060721A>T , CM000681.2:g.49060721A>T GRCh38
NC_000019.9:g.49563978A>T , CM000681.1:g.49563978A>T GRCh37
NC_000019.8:g.54255790A>T NCBI36
NG_016289.1:g.8147T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+1034T>A ENSP00000470689.1:n.243+1034T>A
XM_011527575.1:c.32T>A XP_011525877.1:p.Leu11Gln
XR_001753693.1:n.879+443T>A
Search 100 bp 5'
Search 100 bp 3'