Canonical Allele Identifier: CA309446054
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs749842698
MyVariant Identifiers: chr19:g.49564148T>G (hg19) chr19:g.49060891T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060891T>G , CM000681.2:g.49060891T>G GRCh38
NC_000019.9:g.49564148T>G , CM000681.1:g.49564148T>G GRCh37
NC_000019.8:g.54255960T>G NCBI36
NG_016289.1:g.7977A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+864A>C ENSP00000470689.1:n.243+864A>C
XM_011527575.1:c.-139A>C XP_011525877.1:n.-139A>C
XR_001753693.1:n.879+273A>C
XR_001753694.1:n.880-82A>C
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