Canonical Allele Identifier: CA1989971532
Gene: TYR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89284718A= , CM000673.2:g.89284718A= GRCh38
NC_000011.9:g.89017886A= , CM000673.1:g.89017886A= GRCh37
NC_000011.8:g.88657534A= NCBI36
NG_008748.1:g.111847A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.1185-55A= MANE Select ENSP00000263321.4:n.1185-55A=
ENST00000263321.5:c.1185-55A= ENSP00000263321.4:n.1185-55A=
ENST00000528243.1:n.183-55A=
NM_000372.4:c.1185-55A= NP_000363.1:n.1185-55A=
XM_011542970.1:c.1185-55A= XP_011541272.1:n.1185-55A=
XM_011542970.2:c.1185-55A= XP_011541272.1:n.1185-55A=
XR_001748321.1:n.2456+1316T=
XR_001748322.1:n.2457+1316T=
NM_000372.5:c.1185-55A= MANE Select NP_000363.1:n.1185-55A=
Search 100 bp 5'
Search 100 bp 3'