Canonical Allele Identifier: CA508089731
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564179G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060922G>C , CM000681.2:g.49060922G>C GRCh38
NC_000019.9:g.49564179G>C , CM000681.1:g.49564179G>C GRCh37
NC_000019.8:g.54255991G>C NCBI36
NG_016289.1:g.7946C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+833C>G ENSP00000470689.1:n.243+833C>G
XM_011527575.1:c.-170C>G XP_011525877.1:n.-170C>G
XR_001753693.1:n.879+242C>G
XR_001753694.1:n.880-113C>G
Search 100 bp 5'
Search 100 bp 3'