Canonical Allele Identifier: CA6221111
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs747095957

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178405T>C , CM000673.2:g.89178405T>C GRCh38
NC_000011.9:g.88911573T>C , CM000673.1:g.88911573T>C GRCh37
NC_000011.8:g.88551221T>C NCBI36
NG_008748.1:g.5534T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.452T>C MANE Select ENSP00000263321.4:p.Ile151Thr
ENST00000263321.5:c.452T>C ENSP00000263321.4:p.Ile151Thr
ENST00000526139.1:n.513T>C
NM_000372.4:c.452T>C NP_000363.1:p.Ile151Thr
XM_011542970.1:c.452T>C XP_011541272.1:p.Ile151Thr
XM_011542970.2:c.452T>C XP_011541272.1:p.Ile151Thr
XR_001748321.1:n.2718-64872A>G
XR_001748322.1:n.2733-64872A>G
NM_000372.5:c.452T>C MANE Select NP_000363.1:p.Ile151Thr