Canonical Allele Identifier: CA508278669
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564649T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061392T>C , CM000681.2:g.49061392T>C GRCh38
NC_000019.9:g.49564649T>C , CM000681.1:g.49564649T>C GRCh37
NC_000019.8:g.54256461T>C NCBI36
NG_016289.1:g.7476A>G

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.606A>G NP_006170.1:p.Thr202=
XM_005258962.2:c.606A>G XP_005259019.1:p.Thr202=
XM_006723232.2:c.606A>G XP_006723295.1:p.Thr202=
XM_011527008.1:c.636A>G XP_011525310.1:p.Thr212=
XM_011527009.1:c.606A>G XP_011525311.1:p.Thr202=
XM_011527010.1:c.606A>G XP_011525312.1:p.Thr202=
XM_005258962.3:c.606A>G XP_005259019.1:p.Thr202=
XM_006723232.3:c.606A>G XP_006723295.1:p.Thr202=
XM_011527008.2:c.636A>G XP_011525310.1:p.Thr212=
XM_011527009.2:c.606A>G XP_011525311.1:p.Thr202=
XM_011527010.2:c.606A>G XP_011525312.1:p.Thr202=
XR_001753693.1:n.651A>G
XR_001753694.1:n.651A>G
ENST00000593537.1:n.606A>G ENSP00000469455.1:p.Thr202=
ENST00000599795.5:c.243+363A>G ENSP00000470689.1:p.=