Canonical Allele Identifier: CA508089676
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564163G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060906G>C , CM000681.2:g.49060906G>C GRCh38
NC_000019.9:g.49564163G>C , CM000681.1:g.49564163G>C GRCh37
NC_000019.8:g.54255975G>C NCBI36
NG_016289.1:g.7962C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+849C>G ENSP00000470689.1:n.243+849C>G
XM_011527575.1:c.-154C>G XP_011525877.1:n.-154C>G
XR_001753693.1:n.879+258C>G
XR_001753694.1:n.880-97C>G