Canonical Allele Identifier: CA508089527
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564116G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060859G>C , CM000681.2:g.49060859G>C GRCh38
NC_000019.9:g.49564116G>C , CM000681.1:g.49564116G>C GRCh37
NC_000019.8:g.54255928G>C NCBI36
NG_016289.1:g.8009C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+896C>G ENSP00000470689.1:n.243+896C>G
XM_011527575.1:c.-107C>G XP_011525877.1:n.-107C>G
XR_001753693.1:n.879+305C>G
XR_001753694.1:n.880-50C>G