Canonical Allele Identifier: CA226290812
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs764002598

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178722C>T , CM000673.2:g.89178722C>T GRCh38
NC_000011.9:g.88911890C>T , CM000673.1:g.88911890C>T GRCh37
NC_000011.8:g.88551538C>T NCBI36
NG_008748.1:g.5851C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.769C>T MANE Select ENSP00000263321.4:p.Pro257Ser
ENST00000263321.5:c.769C>T ENSP00000263321.4:p.Pro257Ser
ENST00000526139.1:n.830C>T
NM_000372.4:c.769C>T NP_000363.1:p.Pro257Ser
XM_011542970.1:c.769C>T XP_011541272.1:p.Pro257Ser
XM_011542970.2:c.769C>T XP_011541272.1:p.Pro257Ser
XR_001748321.1:n.2718-65189G>A
XR_001748322.1:n.2733-65189G>A
NM_000372.5:c.769C>T MANE Select NP_000363.1:p.Pro257Ser