Canonical Allele Identifier: CA1948012673
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172199A= , CM000673.2:g.2172199A= GRCh38
NC_000011.9:g.2193429A= , CM000673.1:g.2193429A= GRCh37
NC_000011.8:g.2150005A= NCBI36
NG_008128.1:g.4607T=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-413T= XP_011518637.1:n.-413T=