Canonical Allele Identifier: CA1989920830
Gene: TYR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178549A= , CM000673.2:g.89178549A= GRCh38
NC_000011.9:g.88911717A= , CM000673.1:g.88911717A= GRCh37
NC_000011.8:g.88551365A= NCBI36
NG_008748.1:g.5678A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.596A= MANE Select ENSP00000263321.4:p.Asp199=
ENST00000263321.5:c.596A= ENSP00000263321.4:p.Asp199=
ENST00000526139.1:n.657A=
NM_000372.4:c.596A= NP_000363.1:p.Asp199=
XM_011542970.1:c.596A= XP_011541272.1:p.Asp199=
XM_011542970.2:c.596A= XP_011541272.1:p.Asp199=
XR_001748321.1:n.2718-65016T=
XR_001748322.1:n.2733-65016T=
NM_000372.5:c.596A= MANE Select NP_000363.1:p.Asp199=