Canonical Allele Identifier: CA1948012637
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172171C= , CM000673.2:g.2172171C= GRCh38
NC_000011.9:g.2193401C= , CM000673.1:g.2193401C= GRCh37
NC_000011.8:g.2149977C= NCBI36
NG_008128.1:g.4635G=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-385G= XP_011518637.1:n.-385G=