Canonical Allele Identifier: CA1989921744
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs1943264524

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178853C>G , CM000673.2:g.89178853C>G GRCh38
NC_000011.9:g.88912021C>G , CM000673.1:g.88912021C>G GRCh37
NC_000011.8:g.88551669C>G NCBI36
NG_008748.1:g.5982C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.819+81C>G MANE Select ENSP00000263321.4:n.819+81C>G
ENST00000263321.5:c.819+81C>G ENSP00000263321.4:n.819+81C>G
ENST00000526139.1:n.880+81C>G
NM_000372.4:c.819+81C>G NP_000363.1:n.819+81C>G
XM_011542970.1:c.819+81C>G XP_011541272.1:n.819+81C>G
XM_011542970.2:c.819+81C>G XP_011541272.1:n.819+81C>G
XR_001748321.1:n.2718-65320G>C
XR_001748322.1:n.2733-65320G>C
NM_000372.5:c.819+81C>G MANE Select NP_000363.1:n.819+81C>G