Canonical Allele Identifier: CA2611984629
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2171894-T-C
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Genomic Alleles

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

Transcript Alleles

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