Canonical Allele Identifier: CA508089511
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564111A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060854A>C , CM000681.2:g.49060854A>C GRCh38
NC_000019.9:g.49564111A>C , CM000681.1:g.49564111A>C GRCh37
NC_000019.8:g.54255923A>C NCBI36
NG_016289.1:g.8014T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+901T>G ENSP00000470689.1:n.243+901T>G
XM_011527575.1:c.-102T>G XP_011525877.1:n.-102T>G
XR_001753693.1:n.879+310T>G
XR_001753694.1:n.880-45T>G