Canonical Allele Identifier: CA508089493

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564106T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060849T>A , CM000681.2:g.49060849T>A	GRCh38
NC_000019.9:g.49564106T>A , CM000681.1:g.49564106T>A	GRCh37
NC_000019.8:g.54255918T>A	NCBI36
NG_016289.1:g.8019A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+906A>T	ENSP00000470689.1:n.243+906A>T
XM_011527575.1:c.-97A>T	XP_011525877.1:n.-97A>T
XR_001753693.1:n.879+315A>T
XR_001753694.1:n.880-40A>T