Canonical Allele Identifier: CA382033969
Gene: TYR HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.88911379T>A (hg19) chr11:g.89178211T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178211T>A , CM000673.2:g.89178211T>A GRCh38
NC_000011.9:g.88911379T>A , CM000673.1:g.88911379T>A GRCh37
NC_000011.8:g.88551027T>A NCBI36
NG_008748.1:g.5340T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.258T>A MANE Select ENSP00000263321.4:p.Asn86Lys
ENST00000263321.5:c.258T>A ENSP00000263321.4:p.Asn86Lys
ENST00000526139.1:n.319T>A
NM_000372.4:c.258T>A NP_000363.1:p.Asn86Lys
XM_011542970.1:c.258T>A XP_011541272.1:p.Asn86Lys
XM_011542970.2:c.258T>A XP_011541272.1:p.Asn86Lys
XR_001748321.1:n.2718-64678A>T
XR_001748322.1:n.2733-64678A>T
NM_000372.5:c.258T>A MANE Select NP_000363.1:p.Asn86Lys
Search 100 bp 5'
Search 100 bp 3'