Canonical Allele Identifier: CA508088982
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1445946129
gnomAD v2: 19-49563944-T-G
gnomAD v3: 19-49060687-T-G
gnomAD v4: 19-49060687-T-G
MyVariant Identifiers: chr19:g.49563944T>G (hg19) chr19:g.49060687T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060687T>G , CM000681.2:g.49060687T>G GRCh38
NC_000019.9:g.49563944T>G , CM000681.1:g.49563944T>G GRCh37
NC_000019.8:g.54255756T>G NCBI36
NG_016289.1:g.8181A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000599795.5:c.243+1068A>C ENSP00000470689.1:n.243+1068A>C
XM_011527575.1:c.40+26A>C XP_011525877.1:n.40+26A>C
XR_001753693.1:n.879+477A>C
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