Canonical Allele Identifier: CA309445885
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1047063825
gnomAD v2: 19-49563948-G-C
gnomAD v3: 19-49060691-G-C
gnomAD v4: 19-49060691-G-C
MyVariant Identifiers: chr19:g.49563948G>C (hg19) chr19:g.49060691G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060691G>C , CM000681.2:g.49060691G>C GRCh38
NC_000019.9:g.49563948G>C , CM000681.1:g.49563948G>C GRCh37
NC_000019.8:g.54255760G>C NCBI36
NG_016289.1:g.8177C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+1064C>G ENSP00000470689.1:n.243+1064C>G
XM_011527575.1:c.40+22C>G XP_011525877.1:n.40+22C>G
XR_001753693.1:n.879+473C>G
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