Canonical Allele Identifier: CA382035610
Gene: TYR HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.88911928C>A (hg19) chr11:g.89178760C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178760C>A , CM000673.2:g.89178760C>A GRCh38
NC_000011.9:g.88911928C>A , CM000673.1:g.88911928C>A GRCh37
NC_000011.8:g.88551576C>A NCBI36
NG_008748.1:g.5889C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.807C>A MANE Select ENSP00000263321.4:p.Phe269Leu
ENST00000263321.5:c.807C>A ENSP00000263321.4:p.Phe269Leu
ENST00000526139.1:n.868C>A
NM_000372.4:c.807C>A NP_000363.1:p.Phe269Leu
XM_011542970.1:c.807C>A XP_011541272.1:p.Phe269Leu
XM_011542970.2:c.807C>A XP_011541272.1:p.Phe269Leu
XR_001748321.1:n.2718-65227G>T
XR_001748322.1:n.2733-65227G>T
NM_000372.5:c.807C>A MANE Select NP_000363.1:p.Phe269Leu
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