Canonical Allele Identifier: CA1948012596
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172127G= , CM000673.2:g.2172127G= GRCh38
NC_000011.9:g.2193357G= , CM000673.1:g.2193357G= GRCh37
NC_000011.8:g.2149933G= NCBI36
NG_008128.1:g.4679C=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-341C= XP_011518637.1:n.-341C=
XM_011520335.2:c.-341C= XP_011518637.1:n.-341C=