Canonical Allele Identifier: CA1948012399
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171983A= , CM000673.2:g.2171983A= GRCh38
NC_000011.9:g.2193213A= , CM000673.1:g.2193213A= GRCh37
NC_000011.8:g.2149789A= NCBI36
NG_008128.1:g.4823T=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-197T= XP_011518637.1:n.-197T=
XM_011520335.2:c.-197T= XP_011518637.1:n.-197T=