Canonical Allele Identifier: CA508089314

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564048G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060791G>A , CM000681.2:g.49060791G>A	GRCh38
NC_000019.9:g.49564048G>A , CM000681.1:g.49564048G>A	GRCh37
NC_000019.8:g.54255860G>A	NCBI36
NG_016289.1:g.8077C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000599795.5:c.243+964C>T	ENSP00000470689.1:n.243+964C>T
XM_011527575.1:c.-39C>T	XP_011525877.1:n.-39C>T
XR_001753693.1:n.879+373C>T
XR_001753694.1:n.898C>T