Canonical Allele Identifier: CA1989972684
Gene: TYR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89285185T= , CM000673.2:g.89285185T= GRCh38
NC_000011.9:g.89018353T= , CM000673.1:g.89018353T= GRCh37
NC_000011.8:g.88658001T= NCBI36
NG_008748.1:g.112314T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.1366+231T= MANE Select ENSP00000263321.4:n.1366+231T=
ENST00000263321.5:c.1366+231T= ENSP00000263321.4:n.1366+231T=
ENST00000528243.1:n.364+231T=
NM_000372.4:c.1366+231T= NP_000363.1:n.1366+231T=
XM_011542970.1:c.1366+231T= XP_011541272.1:n.1366+231T=
XM_011542970.2:c.1366+231T= XP_011541272.1:n.1366+231T=
XR_001748321.1:n.2456+849A=
XR_001748322.1:n.2457+849A=
NM_000372.5:c.1366+231T= MANE Select NP_000363.1:n.1366+231T=
Search 100 bp 5'
Search 100 bp 3'