Canonical Allele Identifier: CA309446068
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs184616468
gnomAD v2: 19-49564208-G-T
gnomAD v3: 19-49060951-G-T
gnomAD v4: 19-49060951-G-T
MyVariant Identifiers: chr19:g.49564208G>T (hg19) chr19:g.49060951G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060951G>T , CM000681.2:g.49060951G>T GRCh38
NC_000019.9:g.49564208G>T , CM000681.1:g.49564208G>T GRCh37
NC_000019.8:g.54256020G>T NCBI36
NG_016289.1:g.7917C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+804C>A ENSP00000470689.1:n.243+804C>A
XM_011527575.1:c.-199C>A XP_011525877.1:n.-199C>A
XR_001753693.1:n.879+213C>A
XR_001753694.1:n.880-142C>A
Search 100 bp 5'
Search 100 bp 3'