Canonical Allele Identifier: CA1948012447
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172031C= , CM000673.2:g.2172031C= GRCh38
NC_000011.9:g.2193261C= , CM000673.1:g.2193261C= GRCh37
NC_000011.8:g.2149837C= NCBI36
NG_008128.1:g.4775G=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-245G= XP_011518637.1:n.-245G=
XM_011520335.2:c.-245G= XP_011518637.1:n.-245G=