Canonical Allele Identifier: CA1989972482
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89285035C= , CM000673.2:g.89285035C= GRCh38
NC_000011.9:g.89018203C= , CM000673.1:g.89018203C= GRCh37
NC_000011.8:g.88657851C= NCBI36
NG_008748.1:g.112164C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.1366+81C= MANE Select ENSP00000263321.4:n.1366+81C=
ENST00000263321.5:c.1366+81C= ENSP00000263321.4:n.1366+81C=
ENST00000528243.1:n.364+81C=
NM_000372.4:c.1366+81C= NP_000363.1:n.1366+81C=
XM_011542970.1:c.1366+81C= XP_011541272.1:n.1366+81C=
XM_011542970.2:c.1366+81C= XP_011541272.1:n.1366+81C=
XR_001748321.1:n.2456+999G=
XR_001748322.1:n.2457+999G=
NM_000372.5:c.1366+81C= MANE Select NP_000363.1:n.1366+81C=
Search 100 bp 5'
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