Canonical Allele Identifier: CA1948012499
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172055G= , CM000673.2:g.2172055G= GRCh38
NC_000011.9:g.2193285G= , CM000673.1:g.2193285G= GRCh37
NC_000011.8:g.2149861G= NCBI36
NG_008128.1:g.4751C=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-269C= XP_011518637.1:n.-269C=
XM_011520335.2:c.-269C= XP_011518637.1:n.-269C=