Canonical Allele Identifier: CA1989921705
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178813C= , CM000673.2:g.89178813C= GRCh38
NC_000011.9:g.88911981C= , CM000673.1:g.88911981C= GRCh37
NC_000011.8:g.88551629C= NCBI36
NG_008748.1:g.5942C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.819+41C= MANE Select ENSP00000263321.4:n.819+41C=
ENST00000263321.5:c.819+41C= ENSP00000263321.4:n.819+41C=
ENST00000526139.1:n.880+41C=
NM_000372.4:c.819+41C= NP_000363.1:n.819+41C=
XM_011542970.1:c.819+41C= XP_011541272.1:n.819+41C=
XM_011542970.2:c.819+41C= XP_011541272.1:n.819+41C=
XR_001748321.1:n.2718-65280G=
XR_001748322.1:n.2733-65280G=
NM_000372.5:c.819+41C= MANE Select NP_000363.1:n.819+41C=
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