Canonical Allele Identifier: CA508089329

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564052T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060795T>A , CM000681.2:g.49060795T>A	GRCh38
NC_000019.9:g.49564052T>A , CM000681.1:g.49564052T>A	GRCh37
NC_000019.8:g.54255864T>A	NCBI36
NG_016289.1:g.8073A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000599795.5:c.243+960A>T	ENSP00000470689.1:n.243+960A>T
XM_011527575.1:c.-43A>T	XP_011525877.1:n.-43A>T
XR_001753693.1:n.879+369A>T
XR_001753694.1:n.894A>T