Canonical Allele Identifier: CA2611985022
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2172004-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172004A>C , CM000673.2:g.2172004A>C GRCh38
NC_000011.9:g.2193234A>C , CM000673.1:g.2193234A>C GRCh37
NC_000011.8:g.2149810A>C NCBI36
NG_008128.1:g.4802T>G

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-218T>G XP_011518637.1:n.-218T>G
XM_011520335.2:c.-218T>G XP_011518637.1:n.-218T>G