Canonical Allele Identifier: CA681530735
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs1361161554
MyVariant Identifiers: chr11:g.89018289T>C (hg19) chr11:g.89285121T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89285121T>C , CM000673.2:g.89285121T>C GRCh38
NC_000011.9:g.89018289T>C , CM000673.1:g.89018289T>C GRCh37
NC_000011.8:g.88657937T>C NCBI36
NG_008748.1:g.112250T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.1366+167T>C MANE Select ENSP00000263321.4:n.1366+167T>C
ENST00000263321.5:c.1366+167T>C ENSP00000263321.4:n.1366+167T>C
ENST00000528243.1:n.364+167T>C
NM_000372.4:c.1366+167T>C NP_000363.1:n.1366+167T>C
XM_011542970.1:c.1366+167T>C XP_011541272.1:n.1366+167T>C
XM_011542970.2:c.1366+167T>C XP_011541272.1:n.1366+167T>C
XR_001748321.1:n.2456+913A>G
XR_001748322.1:n.2457+913A>G
NM_000372.5:c.1366+167T>C MANE Select NP_000363.1:n.1366+167T>C
Search 100 bp 5'
Search 100 bp 3'