Canonical Allele Identifier: CA508089246

Gene: NTF4

Linked Data

• dbSNP Id: rs1355620729
• MyVariant Identifiers: chr19:g.49564027C>T (hg19) ; chr19:g.49060770C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060770C>T , CM000681.2:g.49060770C>T	GRCh38
NC_000019.9:g.49564027C>T , CM000681.1:g.49564027C>T	GRCh37
NC_000019.8:g.54255839C>T	NCBI36
NG_016289.1:g.8098G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000599795.5:c.243+985G>A	ENSP00000470689.1:n.243+985G>A
XM_011527575.1:c.-18G>A	XP_011525877.1:n.-18G>A
XR_001753693.1:n.879+394G>A
XR_001753694.1:n.919G>A