Canonical Allele Identifier: CA309445941

Gene: NTF4

Linked Data

• dbSNP Id: rs956815911
• MyVariant Identifiers: chr19:g.49564068T>G (hg19) ; chr19:g.49060811T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060811T>G , CM000681.2:g.49060811T>G	GRCh38
NC_000019.9:g.49564068T>G , CM000681.1:g.49564068T>G	GRCh37
NC_000019.8:g.54255880T>G	NCBI36
NG_016289.1:g.8057A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+944A>C	ENSP00000470689.1:n.243+944A>C
XM_011527575.1:c.-59A>C	XP_011525877.1:n.-59A>C
XR_001753693.1:n.879+353A>C
XR_001753694.1:n.880-2A>C