Canonical Allele Identifier: CA1948012529
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs567621677

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172068G>C , CM000673.2:g.2172068G>C GRCh38
NC_000011.9:g.2193298G>C , CM000673.1:g.2193298G>C GRCh37
NC_000011.8:g.2149874G>C NCBI36
NG_008128.1:g.4738C>G

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-282C>G XP_011518637.1:n.-282C>G
XM_011520335.2:c.-282C>G XP_011518637.1:n.-282C>G