Canonical Allele Identifier: CA2615470706
Gene: TYR HGNC NCBI

Linked Data

gnomAD v4: 11-89178896-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89178896C>A , CM000673.2:g.89178896C>A GRCh38
NC_000011.9:g.88912064C>A , CM000673.1:g.88912064C>A GRCh37
NC_000011.8:g.88551712C>A NCBI36
NG_008748.1:g.6025C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263321.6:c.819+124C>A MANE Select ENSP00000263321.4:n.819+124C>A
ENST00000263321.5:c.819+124C>A ENSP00000263321.4:n.819+124C>A
ENST00000526139.1:n.880+124C>A
NM_000372.4:c.819+124C>A NP_000363.1:n.819+124C>A
XM_011542970.1:c.819+124C>A XP_011541272.1:n.819+124C>A
XM_011542970.2:c.819+124C>A XP_011541272.1:n.819+124C>A
XR_001748321.1:n.2718-65363G>T
XR_001748322.1:n.2733-65363G>T
NM_000372.5:c.819+124C>A MANE Select NP_000363.1:n.819+124C>A
Search 100 bp 5'
Search 100 bp 3'