Canonical Allele Identifier: CA508089658
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564158T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060901T>C , CM000681.2:g.49060901T>C GRCh38
NC_000019.9:g.49564158T>C , CM000681.1:g.49564158T>C GRCh37
NC_000019.8:g.54255970T>C NCBI36
NG_016289.1:g.7967A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+854A>G ENSP00000470689.1:n.243+854A>G
XM_011527575.1:c.-149A>G XP_011525877.1:n.-149A>G
XR_001753693.1:n.879+263A>G
XR_001753694.1:n.880-92A>G