Canonical Allele Identifier: CA6221370
Gene: TYR HGNC NCBI

Linked Data

dbSNP Id: rs773164767
ExAC: 11:89017904 A / G
gnomAD v2: 11-89017904-A-G
gnomAD v3: 11-89284736-A-G
gnomAD v4: 11-89284736-A-G
MyVariant Identifiers: chr11:g.89017904A>G (hg19) chr11:g.89284736A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89284736A>G , CM000673.2:g.89284736A>G GRCh38
NC_000011.9:g.89017904A>G , CM000673.1:g.89017904A>G GRCh37
NC_000011.8:g.88657552A>G NCBI36
NG_008748.1:g.111865A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263321.6:c.1185-37A>G MANE Select ENSP00000263321.4:n.1185-37A>G
ENST00000263321.5:c.1185-37A>G ENSP00000263321.4:n.1185-37A>G
ENST00000528243.1:n.183-37A>G
NM_000372.4:c.1185-37A>G NP_000363.1:n.1185-37A>G
XM_011542970.1:c.1185-37A>G XP_011541272.1:n.1185-37A>G
XM_011542970.2:c.1185-37A>G XP_011541272.1:n.1185-37A>G
XR_001748321.1:n.2456+1298T>C
XR_001748322.1:n.2457+1298T>C
NM_000372.5:c.1185-37A>G MANE Select NP_000363.1:n.1185-37A>G
Search 100 bp 5'
Search 100 bp 3'