Canonical Allele Identifier: CA508089741
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1343548000
gnomAD v2: 19-49564181-C-T
gnomAD v3: 19-49060924-C-T
gnomAD v4: 19-49060924-C-T
MyVariant Identifiers: chr19:g.49564181C>T (hg19) chr19:g.49060924C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060924C>T , CM000681.2:g.49060924C>T GRCh38
NC_000019.9:g.49564181C>T , CM000681.1:g.49564181C>T GRCh37
NC_000019.8:g.54255993C>T NCBI36
NG_016289.1:g.7944G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+831G>A ENSP00000470689.1:n.243+831G>A
XM_011527575.1:c.-172G>A XP_011525877.1:n.-172G>A
XR_001753693.1:n.879+240G>A
XR_001753694.1:n.880-115G>A
Search 100 bp 5'
Search 100 bp 3'