Canonical Allele Identifier: CA508088999
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060693-C-T
MyVariant Identifiers: chr19:g.49563950C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060693C>T , CM000681.2:g.49060693C>T GRCh38
NC_000019.9:g.49563950C>T , CM000681.1:g.49563950C>T GRCh37
NC_000019.8:g.54255762C>T NCBI36
NG_016289.1:g.8175G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000599795.5:c.243+1062G>A ENSP00000470689.1:n.243+1062G>A
XM_011527575.1:c.40+20G>A XP_011525877.1:n.40+20G>A
XR_001753693.1:n.879+471G>A
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