Canonical Allele Identifier: CA508089721
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564177A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060920A>C , CM000681.2:g.49060920A>C GRCh38
NC_000019.9:g.49564177A>C , CM000681.1:g.49564177A>C GRCh37
NC_000019.8:g.54255989A>C NCBI36
NG_016289.1:g.7948T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+835T>G ENSP00000470689.1:n.243+835T>G
XM_011527575.1:c.-168T>G XP_011525877.1:n.-168T>G
XR_001753693.1:n.879+244T>G
XR_001753694.1:n.880-111T>G
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