Canonical Allele Identifier: CA382035841
Gene: TYR HGNC NCBI

Linked Data

gnomAD v4: 11-89191284-C-G
MyVariant Identifiers: chr11:g.88924452C>G (hg19) chr11:g.89191284C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89191284C>G , CM000673.2:g.89191284C>G GRCh38
NC_000011.9:g.88924452C>G , CM000673.1:g.88924452C>G GRCh37
NC_000011.8:g.88564100C>G NCBI36
NG_008748.1:g.18413C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.902C>G MANE Select ENSP00000263321.4:p.Pro301Arg
ENST00000263321.5:c.902C>G ENSP00000263321.4:p.Pro301Arg
ENST00000526139.1:n.963C>G
NM_000372.4:c.902C>G NP_000363.1:p.Pro301Arg
XM_011542970.1:c.902C>G XP_011541272.1:p.Pro301Arg
XM_011542970.2:c.902C>G XP_011541272.1:p.Pro301Arg
XR_001748321.1:n.2718-77751G>C
XR_001748322.1:n.2733-77751G>C
NM_000372.5:c.902C>G MANE Select NP_000363.1:p.Pro301Arg
Search 100 bp 5'
Search 100 bp 3'