Canonical Allele Identifier: CA681559804
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs1469039930
MyVariant Identifiers: chr11:g.88912075C>G (hg19) chr11:g.89178907C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178907C>G , CM000673.2:g.89178907C>G GRCh38
NC_000011.9:g.88912075C>G , CM000673.1:g.88912075C>G GRCh37
NC_000011.8:g.88551723C>G NCBI36
NG_008748.1:g.6036C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.819+135C>G MANE Select ENSP00000263321.4:n.819+135C>G
ENST00000263321.5:c.819+135C>G ENSP00000263321.4:n.819+135C>G
ENST00000526139.1:n.880+135C>G
NM_000372.4:c.819+135C>G NP_000363.1:n.819+135C>G
XM_011542970.1:c.819+135C>G XP_011541272.1:n.819+135C>G
XM_011542970.2:c.819+135C>G XP_011541272.1:n.819+135C>G
XR_001748321.1:n.2718-65374G>C
XR_001748322.1:n.2733-65374G>C
NM_000372.5:c.819+135C>G MANE Select NP_000363.1:n.819+135C>G
Search 100 bp 5'
Search 100 bp 3'