Canonical Allele Identifier: CA508089001
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060694-A-T
MyVariant Identifiers: chr19:g.49563951A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060694A>T , CM000681.2:g.49060694A>T GRCh38
NC_000019.9:g.49563951A>T , CM000681.1:g.49563951A>T GRCh37
NC_000019.8:g.54255763A>T NCBI36
NG_016289.1:g.8174T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000599795.5:c.243+1061T>A ENSP00000470689.1:n.243+1061T>A
XM_011527575.1:c.40+19T>A XP_011525877.1:n.40+19T>A
XR_001753693.1:n.879+470T>A
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