Canonical Allele Identifier: CA508089816
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1426767412
gnomAD v4: 19-49060945-G-A
MyVariant Identifiers: chr19:g.49564202G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060945G>A , CM000681.2:g.49060945G>A GRCh38
NC_000019.9:g.49564202G>A , CM000681.1:g.49564202G>A GRCh37
NC_000019.8:g.54256014G>A NCBI36
NG_016289.1:g.7923C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+810C>T ENSP00000470689.1:n.243+810C>T
XM_011527575.1:c.-193C>T XP_011525877.1:n.-193C>T
XR_001753693.1:n.879+219C>T
XR_001753694.1:n.880-136C>T
Search 100 bp 5'
Search 100 bp 3'