Canonical Allele Identifier: CA1989921132
Gene: TYR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178643C= , CM000673.2:g.89178643C= GRCh38
NC_000011.9:g.88911811C= , CM000673.1:g.88911811C= GRCh37
NC_000011.8:g.88551459C= NCBI36
NG_008748.1:g.5772C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.690C= MANE Select ENSP00000263321.4:p.Asn230=
ENST00000263321.5:c.690C= ENSP00000263321.4:p.Asn230=
ENST00000526139.1:n.751C=
NM_000372.4:c.690C= NP_000363.1:p.Asn230=
XM_011542970.1:c.690C= XP_011541272.1:p.Asn230=
XM_011542970.2:c.690C= XP_011541272.1:p.Asn230=
XR_001748321.1:n.2718-65110G=
XR_001748322.1:n.2733-65110G=
NM_000372.5:c.690C= MANE Select NP_000363.1:p.Asn230=