Canonical Allele Identifier: CA508089990
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1174388918
gnomAD v2: 19-49564250-A-G
gnomAD v3: 19-49060993-A-G
gnomAD v4: 19-49060993-A-G
MyVariant Identifiers: chr19:g.49564250A>G (hg19) chr19:g.49060993A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060993A>G , CM000681.2:g.49060993A>G GRCh38
NC_000019.9:g.49564250A>G , CM000681.1:g.49564250A>G GRCh37
NC_000019.8:g.54256062A>G NCBI36
NG_016289.1:g.7875T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+762T>C ENSP00000470689.1:n.243+762T>C
XR_001753693.1:n.879+171T>C
XR_001753694.1:n.879+171T>C
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