Canonical Allele Identifier: CA1948012632
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172166A= , CM000673.2:g.2172166A= GRCh38
NC_000011.9:g.2193396A= , CM000673.1:g.2193396A= GRCh37
NC_000011.8:g.2149972A= NCBI36
NG_008128.1:g.4640T=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-380T= XP_011518637.1:n.-380T=