Canonical Allele Identifier: CA1948012623
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172151C= , CM000673.2:g.2172151C= GRCh38
NC_000011.9:g.2193381C= , CM000673.1:g.2193381C= GRCh37
NC_000011.8:g.2149957C= NCBI36
NG_008128.1:g.4655G=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-365G= XP_011518637.1:n.-365G=