Canonical Allele Identifier: CA309446109

Gene: NTF4

Linked Data

• dbSNP Id: rs570964409
• gnomAD v2: 19-49564318-T-C
• gnomAD v3: 19-49061061-T-C
• gnomAD v4: 19-49061061-T-C
• MyVariant Identifiers: chr19:g.49564318T>C (hg19) ; chr19:g.49061061T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061061T>C , CM000681.2:g.49061061T>C	GRCh38
NC_000019.9:g.49564318T>C , CM000681.1:g.49564318T>C	GRCh37
NC_000019.8:g.54256130T>C	NCBI36
NG_016289.1:g.7807A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+694A>G	ENSP00000470689.1:n.243+694A>G
XR_001753693.1:n.879+103A>G
XR_001753694.1:n.879+103A>G