Canonical Allele Identifier: CA476320921
Gene: TYR HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.89017974T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89284806T>G , CM000673.2:g.89284806T>G GRCh38
NC_000011.9:g.89017974T>G , CM000673.1:g.89017974T>G GRCh37
NC_000011.8:g.88657622T>G NCBI36
NG_008748.1:g.111935T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.1218T>G MANE Select ENSP00000263321.4:p.Pro406=
ENST00000263321.5:c.1218T>G ENSP00000263321.4:p.Pro406=
ENST00000528243.1:n.216T>G
NM_000372.4:c.1218T>G NP_000363.1:p.Pro406=
XM_011542970.1:c.1218T>G XP_011541272.1:p.Pro406=
XM_011542970.2:c.1218T>G XP_011541272.1:p.Pro406=
XR_001748321.1:n.2456+1228A>C
XR_001748322.1:n.2457+1228A>C
NM_000372.5:c.1218T>G MANE Select NP_000363.1:p.Pro406=
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