Canonical Allele Identifier: CA1948012627
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172160A= , CM000673.2:g.2172160A= GRCh38
NC_000011.9:g.2193390A= , CM000673.1:g.2193390A= GRCh37
NC_000011.8:g.2149966A= NCBI36
NG_008128.1:g.4646T=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-374T= XP_011518637.1:n.-374T=