Canonical Allele Identifier: CA309446001
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs368012525
gnomAD v3: 19-49060842-C-G
gnomAD v4: 19-49060842-C-G
MyVariant Identifiers: chr19:g.49564099C>G (hg19) chr19:g.49060842C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060842C>G , CM000681.2:g.49060842C>G GRCh38
NC_000019.9:g.49564099C>G , CM000681.1:g.49564099C>G GRCh37
NC_000019.8:g.54255911C>G NCBI36
NG_016289.1:g.8026G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+913G>C ENSP00000470689.1:n.243+913G>C
XM_011527575.1:c.-90G>C XP_011525877.1:n.-90G>C
XR_001753693.1:n.879+322G>C
XR_001753694.1:n.880-33G>C
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