Canonical Allele Identifier: CA508089382

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564069C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060812C>G , CM000681.2:g.49060812C>G	GRCh38
NC_000019.9:g.49564069C>G , CM000681.1:g.49564069C>G	GRCh37
NC_000019.8:g.54255881C>G	NCBI36
NG_016289.1:g.8056G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+943G>C	ENSP00000470689.1:n.243+943G>C
XM_011527575.1:c.-60G>C	XP_011525877.1:n.-60G>C
XR_001753693.1:n.879+352G>C
XR_001753694.1:n.880-3G>C