Canonical Allele Identifier: CA1989921866

Gene: TYR

Linked Data

• dbSNP Id: rs1943265236
• gnomAD v4: 11-89178914-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89178914T>C , CM000673.2:g.89178914T>C	GRCh38
NC_000011.9:g.88912082T>C , CM000673.1:g.88912082T>C	GRCh37
NC_000011.8:g.88551730T>C	NCBI36
NG_008748.1:g.6043T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263321.6:c.819+142T>C MANE Select	ENSP00000263321.4:n.819+142T>C
ENST00000263321.5:c.819+142T>C	ENSP00000263321.4:n.819+142T>C
ENST00000526139.1:n.880+142T>C
NM_000372.4:c.819+142T>C	NP_000363.1:n.819+142T>C
XM_011542970.1:c.819+142T>C	XP_011541272.1:n.819+142T>C
XM_011542970.2:c.819+142T>C	XP_011541272.1:n.819+142T>C
XR_001748321.1:n.2718-65381A>G
XR_001748322.1:n.2733-65381A>G
NM_000372.5:c.819+142T>C MANE Select	NP_000363.1:n.819+142T>C