Canonical Allele Identifier: CA1989921724

Gene: TYR

Linked Data

• dbSNP Id: rs1943264357

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178835C>G , CM000673.2:g.89178835C>G	GRCh38
NC_000011.9:g.88912003C>G , CM000673.1:g.88912003C>G	GRCh37
NC_000011.8:g.88551651C>G	NCBI36
NG_008748.1:g.5964C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+63C>G MANE Select	ENSP00000263321.4:n.819+63C>G
ENST00000263321.5:c.819+63C>G	ENSP00000263321.4:n.819+63C>G
ENST00000526139.1:n.880+63C>G
NM_000372.4:c.819+63C>G	NP_000363.1:n.819+63C>G
XM_011542970.1:c.819+63C>G	XP_011541272.1:n.819+63C>G
XM_011542970.2:c.819+63C>G	XP_011541272.1:n.819+63C>G
XR_001748321.1:n.2718-65302G>C
XR_001748322.1:n.2733-65302G>C
NM_000372.5:c.819+63C>G MANE Select	NP_000363.1:n.819+63C>G