Canonical Allele Identifier: CA1989972610
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89285131C= , CM000673.2:g.89285131C= GRCh38
NC_000011.9:g.89018299C= , CM000673.1:g.89018299C= GRCh37
NC_000011.8:g.88657947C= NCBI36
NG_008748.1:g.112260C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.1366+177C= MANE Select ENSP00000263321.4:n.1366+177C=
ENST00000263321.5:c.1366+177C= ENSP00000263321.4:n.1366+177C=
ENST00000528243.1:n.364+177C=
NM_000372.4:c.1366+177C= NP_000363.1:n.1366+177C=
XM_011542970.1:c.1366+177C= XP_011541272.1:n.1366+177C=
XM_011542970.2:c.1366+177C= XP_011541272.1:n.1366+177C=
XR_001748321.1:n.2456+903G=
XR_001748322.1:n.2457+903G=
NM_000372.5:c.1366+177C= MANE Select NP_000363.1:n.1366+177C=
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