Canonical Allele Identifier: CA1948012349
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171953G= , CM000673.2:g.2171953G= GRCh38
NC_000011.9:g.2193183G= , CM000673.1:g.2193183G= GRCh37
NC_000011.8:g.2149759G= NCBI36
NG_008128.1:g.4853C=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-167C= XP_011518637.1:n.-167C=
XM_011520335.2:c.-167C= XP_011518637.1:n.-167C=