Canonical Allele Identifier: CA1989972551
Gene: TYR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89285083C= , CM000673.2:g.89285083C= GRCh38
NC_000011.9:g.89018251C= , CM000673.1:g.89018251C= GRCh37
NC_000011.8:g.88657899C= NCBI36
NG_008748.1:g.112212C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.1366+129C= MANE Select ENSP00000263321.4:n.1366+129C=
ENST00000263321.5:c.1366+129C= ENSP00000263321.4:n.1366+129C=
ENST00000528243.1:n.364+129C=
NM_000372.4:c.1366+129C= NP_000363.1:n.1366+129C=
XM_011542970.1:c.1366+129C= XP_011541272.1:n.1366+129C=
XM_011542970.2:c.1366+129C= XP_011541272.1:n.1366+129C=
XR_001748321.1:n.2456+951G=
XR_001748322.1:n.2457+951G=
NM_000372.5:c.1366+129C= MANE Select NP_000363.1:n.1366+129C=
Search 100 bp 5'
Search 100 bp 3'