Canonical Allele Identifier: CA674605149
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1346245721
gnomAD v3: 11-2171956-G-A
gnomAD v4: 11-2171956-G-A
MyVariant Identifiers: chr11:g.2193186G>A (hg19) chr11:g.2171956G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171956G>A , CM000673.2:g.2171956G>A GRCh38
NC_000011.9:g.2193186G>A , CM000673.1:g.2193186G>A GRCh37
NC_000011.8:g.2149762G>A NCBI36
NG_008128.1:g.4850C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-170C>T XP_011518637.1:n.-170C>T
XM_011520335.2:c.-170C>T XP_011518637.1:n.-170C>T
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