Canonical Allele Identifier: CA508089860
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1488473827
gnomAD v2: 19-49564214-C-G
gnomAD v3: 19-49060957-C-G
gnomAD v4: 19-49060957-C-G
MyVariant Identifiers: chr19:g.49564214C>G (hg19) chr19:g.49060957C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060957C>G , CM000681.2:g.49060957C>G GRCh38
NC_000019.9:g.49564214C>G , CM000681.1:g.49564214C>G GRCh37
NC_000019.8:g.54256026C>G NCBI36
NG_016289.1:g.7911G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+798G>C ENSP00000470689.1:n.243+798G>C
XM_011527575.1:c.-205G>C XP_011525877.1:n.-205G>C
XR_001753693.1:n.879+207G>C
XR_001753694.1:n.880-148G>C
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