Canonical Allele Identifier: CA226650376
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs927791789
MyVariant Identifiers: chr11:g.89018362C>A (hg19) chr11:g.89285194C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89285194C>A , CM000673.2:g.89285194C>A GRCh38
NC_000011.9:g.89018362C>A , CM000673.1:g.89018362C>A GRCh37
NC_000011.8:g.88658010C>A NCBI36
NG_008748.1:g.112323C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.1366+240C>A MANE Select ENSP00000263321.4:n.1366+240C>A
ENST00000263321.5:c.1366+240C>A ENSP00000263321.4:n.1366+240C>A
ENST00000528243.1:n.364+240C>A
NM_000372.4:c.1366+240C>A NP_000363.1:n.1366+240C>A
XM_011542970.1:c.1366+240C>A XP_011541272.1:n.1366+240C>A
XM_011542970.2:c.1366+240C>A XP_011541272.1:n.1366+240C>A
XR_001748321.1:n.2456+840G>T
XR_001748322.1:n.2457+840G>T
NM_000372.5:c.1366+240C>A MANE Select NP_000363.1:n.1366+240C>A
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