Canonical Allele Identifier: CA508089427
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1431065400
gnomAD v3: 19-49060827-T-A
gnomAD v4: 19-49060827-T-A
MyVariant Identifiers: chr19:g.49564084T>A (hg19) chr19:g.49060827T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060827T>A , CM000681.2:g.49060827T>A GRCh38
NC_000019.9:g.49564084T>A , CM000681.1:g.49564084T>A GRCh37
NC_000019.8:g.54255896T>A NCBI36
NG_016289.1:g.8041A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+928A>T ENSP00000470689.1:n.243+928A>T
XM_011527575.1:c.-75A>T XP_011525877.1:n.-75A>T
XR_001753693.1:n.879+337A>T
XR_001753694.1:n.880-18A>T
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