Canonical Allele Identifier: CA15950971
Gene: NTF4 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.49060867A>G
GRCh37 chr19:g.49564124A>G
gnomAD v2:
19:49564124 A / G
gnomAD v3:
19:49060867 A / G
gnomAD v4:
chr19-49060867-A-G
Joint Max Group AF 0.20636979 (AMR)
Genomes Max Group AF 0.20432594 (AMR)
Exomes Max Group AF 0.2062908 (AMR)
dbSNP:
11669977
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060867A>G , CM000681.2:g.49060867A>G GRCh38
NC_000019.9:g.49564124A>G , CM000681.1:g.49564124A>G GRCh37
NC_000019.8:g.54255936A>G NCBI36
NG_016289.1:g.8001T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+888T>C ENSP00000470689.1:n.243+888T>C
XM_011527575.1:c.-115T>C XP_011525877.1:n.-115T>C
XR_001753693.1:n.879+297T>C
XR_001753694.1:n.880-58T>C
Search 100 bp 5'
Search 100 bp 3'