Canonical Allele Identifier: CA13489136
Gene: TYR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1393350

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89277878G>A , CM000673.2:g.89277878G>A GRCh38
NC_000011.9:g.89011046G>A , CM000673.1:g.89011046G>A GRCh37
NC_000011.8:g.88650694G>A NCBI36
NG_008748.1:g.105007G>A

Transcript Alleles

HGVS Amino-acid change
NM_000372.4:c.1185-6895G>A VV NP_000363.1:p.=
XM_011542970.1:c.1185-6895G>A XP_011541272.1:p.=
XM_011542970.2:c.1185-6895G>A XP_011541272.1:p.=
XR_001748321.1:n.2457-943C>T
XR_001748322.1:n.2458-1069C>T
NM_000372.5:c.1185-6895G>A VV MANE Preferred NP_000363.1:p.=
ENST00000263321.5:c.1185-6895G>A ENSP00000263321.4:p.=