Canonical Allele Identifier: CA1989972692
Gene: TYR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89285191G= , CM000673.2:g.89285191G= GRCh38
NC_000011.9:g.89018359G= , CM000673.1:g.89018359G= GRCh37
NC_000011.8:g.88658007G= NCBI36
NG_008748.1:g.112320G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.1366+237G= MANE Select ENSP00000263321.4:n.1366+237G=
ENST00000263321.5:c.1366+237G= ENSP00000263321.4:n.1366+237G=
ENST00000528243.1:n.364+237G=
NM_000372.4:c.1366+237G= NP_000363.1:n.1366+237G=
XM_011542970.1:c.1366+237G= XP_011541272.1:n.1366+237G=
XM_011542970.2:c.1366+237G= XP_011541272.1:n.1366+237G=
XR_001748321.1:n.2456+843C=
XR_001748322.1:n.2457+843C=
NM_000372.5:c.1366+237G= MANE Select NP_000363.1:n.1366+237G=
Search 100 bp 5'
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