Canonical Allele Identifier: CA226290256
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs749784786

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178203T>C , CM000673.2:g.89178203T>C GRCh38
NC_000011.9:g.88911371T>C , CM000673.1:g.88911371T>C GRCh37
NC_000011.8:g.88551019T>C NCBI36
NG_008748.1:g.5332T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.250T>C MANE Select ENSP00000263321.4:p.Phe84Leu
ENST00000263321.5:c.250T>C ENSP00000263321.4:p.Phe84Leu
ENST00000526139.1:n.311T>C
NM_000372.4:c.250T>C NP_000363.1:p.Phe84Leu
XM_011542970.1:c.250T>C XP_011541272.1:p.Phe84Leu
XM_011542970.2:c.250T>C XP_011541272.1:p.Phe84Leu
XR_001748321.1:n.2718-64670A>G
XR_001748322.1:n.2733-64670A>G
NM_000372.5:c.250T>C MANE Select NP_000363.1:p.Phe84Leu