Canonical Allele Identifier: CA2611984590
Gene: TH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171884_2171885insCCTTACATCCCCCACCC , CM000673.2:g.2171884_2171885insCCTTACATCCCCCACCC GRCh38
NC_000011.9:g.2193114_2193115insCCTTACATCCCCCACCC , CM000673.1:g.2193114_2193115insCCTTACATCCCCCACCC GRCh37
NC_000011.8:g.2149690_2149691insCCTTACATCCCCCACCC NCBI36
NG_008128.1:g.4921_4922insGGGTGGGGGATGTAAGG

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-99_-98insGGGTGGGGGATGTAAGG XP_011518637.1:n.-99_-98insGGGTGGGGGATGTAAGG
XM_011520335.2:c.-99_-98insGGGTGGGGGATGTAAGG XP_011518637.1:n.-99_-98insGGGTGGGGGATGTAAGG