Canonical Allele Identifier: CA1948012583
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172117A= , CM000673.2:g.2172117A= GRCh38
NC_000011.9:g.2193347A= , CM000673.1:g.2193347A= GRCh37
NC_000011.8:g.2149923A= NCBI36
NG_008128.1:g.4689T=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-331T= XP_011518637.1:n.-331T=
XM_011520335.2:c.-331T= XP_011518637.1:n.-331T=