Canonical Allele Identifier: CA508089773

Gene: NTF4

Linked Data

• gnomAD v4: 19-49060933-A-C
• MyVariant Identifiers: chr19:g.49564190A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49060933A>C , CM000681.2:g.49060933A>C	GRCh38
NC_000019.9:g.49564190A>C , CM000681.1:g.49564190A>C	GRCh37
NC_000019.8:g.54256002A>C	NCBI36
NG_016289.1:g.7935T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000599795.5:c.243+822T>G	ENSP00000470689.1:n.243+822T>G
XM_011527575.1:c.-181T>G	XP_011525877.1:n.-181T>G
XR_001753693.1:n.879+231T>G
XR_001753694.1:n.880-124T>G