Canonical Allele Identifier: CA1948012613
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172141C= , CM000673.2:g.2172141C= GRCh38
NC_000011.9:g.2193371C= , CM000673.1:g.2193371C= GRCh37
NC_000011.8:g.2149947C= NCBI36
NG_008128.1:g.4665G=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-355G= XP_011518637.1:n.-355G=