Canonical Allele Identifier: CA508089552
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564124A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060867A>C , CM000681.2:g.49060867A>C GRCh38
NC_000019.9:g.49564124A>C , CM000681.1:g.49564124A>C GRCh37
NC_000019.8:g.54255936A>C NCBI36
NG_016289.1:g.8001T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+888T>G ENSP00000470689.1:n.243+888T>G
XM_011527575.1:c.-115T>G XP_011525877.1:n.-115T>G
XR_001753693.1:n.879+297T>G
XR_001753694.1:n.880-58T>G