Canonical Allele Identifier: CA1989971542
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89284721T= , CM000673.2:g.89284721T= GRCh38
NC_000011.9:g.89017889T= , CM000673.1:g.89017889T= GRCh37
NC_000011.8:g.88657537T= NCBI36
NG_008748.1:g.111850T=

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.1185-52T= MANE Select ENSP00000263321.4:n.1185-52T=
ENST00000263321.5:c.1185-52T= ENSP00000263321.4:n.1185-52T=
ENST00000528243.1:n.183-52T=
NM_000372.4:c.1185-52T= NP_000363.1:n.1185-52T=
XM_011542970.1:c.1185-52T= XP_011541272.1:n.1185-52T=
XM_011542970.2:c.1185-52T= XP_011541272.1:n.1185-52T=
XR_001748321.1:n.2456+1313A=
XR_001748322.1:n.2457+1313A=
NM_000372.5:c.1185-52T= MANE Select NP_000363.1:n.1185-52T=
Search 100 bp 5'
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