Canonical Allele Identifier: CA1989921874
Gene: TYR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178918T= , CM000673.2:g.89178918T= GRCh38
NC_000011.9:g.88912086T= , CM000673.1:g.88912086T= GRCh37
NC_000011.8:g.88551734T= NCBI36
NG_008748.1:g.6047T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.819+146T= MANE Select ENSP00000263321.4:n.819+146T=
ENST00000263321.5:c.819+146T= ENSP00000263321.4:n.819+146T=
ENST00000526139.1:n.880+146T=
NM_000372.4:c.819+146T= NP_000363.1:n.819+146T=
XM_011542970.1:c.819+146T= XP_011541272.1:n.819+146T=
XM_011542970.2:c.819+146T= XP_011541272.1:n.819+146T=
XR_001748321.1:n.2718-65385A=
XR_001748322.1:n.2733-65385A=
NM_000372.5:c.819+146T= MANE Select NP_000363.1:n.819+146T=
Search 100 bp 5'
Search 100 bp 3'