Canonical Allele Identifier: CA508089790
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564194G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060937G>C , CM000681.2:g.49060937G>C GRCh38
NC_000019.9:g.49564194G>C , CM000681.1:g.49564194G>C GRCh37
NC_000019.8:g.54256006G>C NCBI36
NG_016289.1:g.7931C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000599795.5:c.243+818C>G ENSP00000470689.1:n.243+818C>G
XM_011527575.1:c.-185C>G XP_011525877.1:n.-185C>G
XR_001753693.1:n.879+227C>G
XR_001753694.1:n.880-128C>G
Search 100 bp 5'
Search 100 bp 3'