Canonical Allele Identifier: CA508089804
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1278791893
gnomAD v2: 19-49564198-G-T
gnomAD v3: 19-49060941-G-T
gnomAD v4: 19-49060941-G-T
MyVariant Identifiers: chr19:g.49564198G>T (hg19) chr19:g.49060941G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060941G>T , CM000681.2:g.49060941G>T GRCh38
NC_000019.9:g.49564198G>T , CM000681.1:g.49564198G>T GRCh37
NC_000019.8:g.54256010G>T NCBI36
NG_016289.1:g.7927C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+814C>A ENSP00000470689.1:n.243+814C>A
XM_011527575.1:c.-189C>A XP_011525877.1:n.-189C>A
XR_001753693.1:n.879+223C>A
XR_001753694.1:n.880-132C>A
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