Canonical Allele Identifier: CA309445996
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs895576560
gnomAD v2: 19-49564080-A-G
gnomAD v3: 19-49060823-A-G
gnomAD v4: 19-49060823-A-G
MyVariant Identifiers: chr19:g.49564080A>G (hg19) chr19:g.49060823A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060823A>G , CM000681.2:g.49060823A>G GRCh38
NC_000019.9:g.49564080A>G , CM000681.1:g.49564080A>G GRCh37
NC_000019.8:g.54255892A>G NCBI36
NG_016289.1:g.8045T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+932T>C ENSP00000470689.1:n.243+932T>C
XM_011527575.1:c.-71T>C XP_011525877.1:n.-71T>C
XR_001753693.1:n.879+341T>C
XR_001753694.1:n.880-14T>C
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