Canonical Allele Identifier: CA216230575
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs926009450
MyVariant Identifiers: chr11:g.2193338A>T (hg19) chr11:g.2172108A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172108A>T , CM000673.2:g.2172108A>T GRCh38
NC_000011.9:g.2193338A>T , CM000673.1:g.2193338A>T GRCh37
NC_000011.8:g.2149914A>T NCBI36
NG_008128.1:g.4698T>A

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-322T>A XP_011518637.1:n.-322T>A
XM_011520335.2:c.-322T>A XP_011518637.1:n.-322T>A
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