Canonical Allele Identifier: CA508089111
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060729-G-A
MyVariant Identifiers: chr19:g.49563986G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060729G>A , CM000681.2:g.49060729G>A GRCh38
NC_000019.9:g.49563986G>A , CM000681.1:g.49563986G>A GRCh37
NC_000019.8:g.54255798G>A NCBI36
NG_016289.1:g.8139C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+1026C>T ENSP00000470689.1:n.243+1026C>T
XM_011527575.1:c.24C>T XP_011525877.1:p.Gly8=
XR_001753693.1:n.879+435C>T
XR_001753694.1:n.960C>T
Search 100 bp 5'
Search 100 bp 3'