Canonical Allele Identifier: CA1948012508
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172059T= , CM000673.2:g.2172059T= GRCh38
NC_000011.9:g.2193289T= , CM000673.1:g.2193289T= GRCh37
NC_000011.8:g.2149865T= NCBI36
NG_008128.1:g.4747A=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-273A= XP_011518637.1:n.-273A=
XM_011520335.2:c.-273A= XP_011518637.1:n.-273A=