Canonical Allele Identifier: CA309446070
Gene: NTF4 HGNC NCBI

Linked Data

dbSNP Id: rs1006574246
gnomAD v2: 19-49564211-T-C
gnomAD v3: 19-49060954-T-C
gnomAD v4: 19-49060954-T-C
MyVariant Identifiers: chr19:g.49564211T>C (hg19) chr19:g.49060954T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060954T>C , CM000681.2:g.49060954T>C GRCh38
NC_000019.9:g.49564211T>C , CM000681.1:g.49564211T>C GRCh37
NC_000019.8:g.54256023T>C NCBI36
NG_016289.1:g.7914A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+801A>G ENSP00000470689.1:n.243+801A>G
XM_011527575.1:c.-202A>G XP_011525877.1:n.-202A>G
XR_001753693.1:n.879+210A>G
XR_001753694.1:n.880-145A>G
Search 100 bp 5'
Search 100 bp 3'