Canonical Allele Identifier: CA2611984628
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2171894-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171894T>G , CM000673.2:g.2171894T>G GRCh38
NC_000011.9:g.2193124T>G , CM000673.1:g.2193124T>G GRCh37
NC_000011.8:g.2149700T>G NCBI36
NG_008128.1:g.4912A>C

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-108A>C XP_011518637.1:n.-108A>C
XM_011520335.2:c.-108A>C XP_011518637.1:n.-108A>C