Canonical Allele Identifier: CA1948012604
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172129T= , CM000673.2:g.2172129T= GRCh38
NC_000011.9:g.2193359T= , CM000673.1:g.2193359T= GRCh37
NC_000011.8:g.2149935T= NCBI36
NG_008128.1:g.4677A=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-343A= XP_011518637.1:n.-343A=
XM_011520335.2:c.-343A= XP_011518637.1:n.-343A=