Canonical Allele Identifier: CA508089086
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1367376498
gnomAD v3: 19-49060720-C-G
gnomAD v4: 19-49060720-C-G
MyVariant Identifiers: chr19:g.49563977C>G (hg19) chr19:g.49060720C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060720C>G , CM000681.2:g.49060720C>G GRCh38
NC_000019.9:g.49563977C>G , CM000681.1:g.49563977C>G GRCh37
NC_000019.8:g.54255789C>G NCBI36
NG_016289.1:g.8148G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+1035G>C ENSP00000470689.1:n.243+1035G>C
XM_011527575.1:c.33G>C XP_011525877.1:p.Leu11=
XR_001753693.1:n.879+444G>C
Search 100 bp 5'
Search 100 bp 3'