Canonical Allele Identifier: CA508089005
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49563952G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060695G>C , CM000681.2:g.49060695G>C GRCh38
NC_000019.9:g.49563952G>C , CM000681.1:g.49563952G>C GRCh37
NC_000019.8:g.54255764G>C NCBI36
NG_016289.1:g.8173C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000599795.5:c.243+1060C>G ENSP00000470689.1:n.243+1060C>G
XM_011527575.1:c.40+18C>G XP_011525877.1:n.40+18C>G
XR_001753693.1:n.879+469C>G
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