Canonical Allele Identifier: CA1630855254
Community Standard Title: NC_000011.10:g.89177755C=
Gene: TYR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89177755C= , CM000673.2:g.89177755C= GRCh38
NC_000011.9:g.88910923C= , CM000673.1:g.88910923C= GRCh37
NC_000011.8:g.88550571C= NCBI36
NG_008748.1:g.4884C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.5:c.-199C= ENSP00000263321.4:n.-199C=
XM_011542970.2:c.-199C= XP_011541272.1:n.-199C=
XR_001748321.1:n.2718-64222G=
XR_001748322.1:n.2733-64222G=