Canonical Allele Identifier: CA382035192
Gene: TYR HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.88911833T>G (hg19) chr11:g.89178665T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178665T>G , CM000673.2:g.89178665T>G GRCh38
NC_000011.9:g.88911833T>G , CM000673.1:g.88911833T>G GRCh37
NC_000011.8:g.88551481T>G NCBI36
NG_008748.1:g.5794T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.712T>G MANE Select ENSP00000263321.4:p.Trp238Gly
ENST00000263321.5:c.712T>G ENSP00000263321.4:p.Trp238Gly
ENST00000526139.1:n.773T>G
NM_000372.4:c.712T>G NP_000363.1:p.Trp238Gly
XM_011542970.1:c.712T>G XP_011541272.1:p.Trp238Gly
XM_011542970.2:c.712T>G XP_011541272.1:p.Trp238Gly
XR_001748321.1:n.2718-65132A>C
XR_001748322.1:n.2733-65132A>C
NM_000372.5:c.712T>G MANE Select NP_000363.1:p.Trp238Gly
Search 100 bp 5'
Search 100 bp 3'