Canonical Allele Identifier: CA508089450

Gene: NTF4

Linked Data

• dbSNP Id: rs2040122466
• gnomAD v4: 19-49060834-A-G
• MyVariant Identifiers: chr19:g.49564091A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060834A>G , CM000681.2:g.49060834A>G	GRCh38
NC_000019.9:g.49564091A>G , CM000681.1:g.49564091A>G	GRCh37
NC_000019.8:g.54255903A>G	NCBI36
NG_016289.1:g.8034T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+921T>C	ENSP00000470689.1:n.243+921T>C
XM_011527575.1:c.-82T>C	XP_011525877.1:n.-82T>C
XR_001753693.1:n.879+330T>C
XR_001753694.1:n.880-25T>C