Canonical Allele Identifier: CA2615470711
Gene: TYR HGNC NCBI

Linked Data

gnomAD v4: 11-89178901-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178901T>A , CM000673.2:g.89178901T>A GRCh38
NC_000011.9:g.88912069T>A , CM000673.1:g.88912069T>A GRCh37
NC_000011.8:g.88551717T>A NCBI36
NG_008748.1:g.6030T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.819+129T>A MANE Select ENSP00000263321.4:n.819+129T>A
ENST00000263321.5:c.819+129T>A ENSP00000263321.4:n.819+129T>A
ENST00000526139.1:n.880+129T>A
NM_000372.4:c.819+129T>A NP_000363.1:n.819+129T>A
XM_011542970.1:c.819+129T>A XP_011541272.1:n.819+129T>A
XM_011542970.2:c.819+129T>A XP_011541272.1:n.819+129T>A
XR_001748321.1:n.2718-65368A>T
XR_001748322.1:n.2733-65368A>T
NM_000372.5:c.819+129T>A MANE Select NP_000363.1:n.819+129T>A
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