Canonical Allele Identifier: CA1948013591
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2173062G= , CM000673.2:g.2173062G= GRCh38
NC_000011.9:g.2194292G= , CM000673.1:g.2194292G= GRCh37
NC_000011.8:g.2150868G= NCBI36
NG_008128.1:g.3744C=

Transcript Alleles

HGVS Amino-acid change
XM_011520335.2:c.-1276C= XP_011518637.1:n.-1276C=