Canonical Allele Identifier: CA508278649
Gene: NTF4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.49564640G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061383G>A , CM000681.2:g.49061383G>A GRCh38
NC_000019.9:g.49564640G>A , CM000681.1:g.49564640G>A GRCh37
NC_000019.8:g.54256452G>A NCBI36
NG_016289.1:g.7485C>T

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.615C>T NP_006170.1:p.Ser205=
XM_005258962.2:c.615C>T XP_005259019.1:p.Ser205=
XM_006723232.2:c.615C>T XP_006723295.1:p.Ser205=
XM_011527008.1:c.645C>T XP_011525310.1:p.Ser215=
XM_011527009.1:c.615C>T XP_011525311.1:p.Ser205=
XM_011527010.1:c.615C>T XP_011525312.1:p.Ser205=
XM_005258962.3:c.615C>T XP_005259019.1:p.Ser205=
XM_006723232.3:c.615C>T XP_006723295.1:p.Ser205=
XM_011527008.2:c.645C>T XP_011525310.1:p.Ser215=
XM_011527009.2:c.615C>T XP_011525311.1:p.Ser205=
XM_011527010.2:c.615C>T XP_011525312.1:p.Ser205=
XR_001753693.1:n.660C>T
XR_001753694.1:n.660C>T
ENST00000593537.1:n.615C>T ENSP00000469455.1:p.Ser205=
ENST00000599795.5:c.243+372C>T ENSP00000470689.1:p.=