Canonical Allele Identifier: CA934421006
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1846274321

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172031del , CM000673.2:g.2172031del GRCh38
NC_000011.9:g.2193261del , CM000673.1:g.2193261del GRCh37
NC_000011.8:g.2149837del NCBI36
NG_008128.1:g.4775del

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-245del XP_011518637.1:n.-245del
XM_011520335.2:c.-245del XP_011518637.1:n.-245del