Canonical Allele Identifier: CA508089325

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564051A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060794A>T , CM000681.2:g.49060794A>T	GRCh38
NC_000019.9:g.49564051A>T , CM000681.1:g.49564051A>T	GRCh37
NC_000019.8:g.54255863A>T	NCBI36
NG_016289.1:g.8074T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+961T>A	ENSP00000470689.1:n.243+961T>A
XM_011527575.1:c.-42T>A	XP_011525877.1:n.-42T>A
XR_001753693.1:n.879+370T>A
XR_001753694.1:n.895T>A