Canonical Allele Identifier: CA508089202
Gene: NTF4 HGNC NCBI

Linked Data

gnomAD v4: 19-49060757-A-C
MyVariant Identifiers: chr19:g.49564014A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060757A>C , CM000681.2:g.49060757A>C GRCh38
NC_000019.9:g.49564014A>C , CM000681.1:g.49564014A>C GRCh37
NC_000019.8:g.54255826A>C NCBI36
NG_016289.1:g.8111T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+998T>G ENSP00000470689.1:n.243+998T>G
XM_011527575.1:c.-5T>G XP_011525877.1:n.-5T>G
XR_001753693.1:n.879+407T>G
XR_001753694.1:n.932T>G
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