Canonical Allele Identifier: CA508089774
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564190A>G (hg19)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+822T>C ENSP00000470689.1:n.243+822T>C
XM_011527575.1:c.-181T>C XP_011525877.1:n.-181T>C
XR_001753693.1:n.879+231T>C
XR_001753694.1:n.880-124T>C
Search 100 bp 5'
Search 100 bp 3'