Canonical Allele Identifier: CA508089596
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564138T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060881T>G , CM000681.2:g.49060881T>G GRCh38
NC_000019.9:g.49564138T>G , CM000681.1:g.49564138T>G GRCh37
NC_000019.8:g.54255950T>G NCBI36
NG_016289.1:g.7987A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+874A>C ENSP00000470689.1:n.243+874A>C
XM_011527575.1:c.-129A>C XP_011525877.1:n.-129A>C
XR_001753693.1:n.879+283A>C
XR_001753694.1:n.880-72A>C
Search 100 bp 5'
Search 100 bp 3'