Canonical Allele Identifier: CA309445917

Gene: NTF4

Linked Data

• dbSNP Id: rs965987955
• gnomAD v2: 19-49564037-T-A
• gnomAD v3: 19-49060780-T-A
• gnomAD v4: 19-49060780-T-A
• MyVariant Identifiers: chr19:g.49564037T>A (hg19) ; chr19:g.49060780T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060780T>A , CM000681.2:g.49060780T>A	GRCh38
NC_000019.9:g.49564037T>A , CM000681.1:g.49564037T>A	GRCh37
NC_000019.8:g.54255849T>A	NCBI36
NG_016289.1:g.8088A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000599795.5:c.243+975A>T	ENSP00000470689.1:n.243+975A>T
XM_011527575.1:c.-28A>T	XP_011525877.1:n.-28A>T
XR_001753693.1:n.879+384A>T
XR_001753694.1:n.909A>T