Canonical Allele Identifier: CA508088955
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49563936A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49060679A>C , CM000681.2:g.49060679A>C GRCh38
NC_000019.9:g.49563936A>C , CM000681.1:g.49563936A>C GRCh37
NC_000019.8:g.54255748A>C NCBI36
NG_016289.1:g.8189T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000599795.5:c.243+1076T>G ENSP00000470689.1:n.243+1076T>G
XM_011527575.1:c.40+34T>G XP_011525877.1:n.40+34T>G
XR_001753693.1:n.879+485T>G