Canonical Allele Identifier: CA216230358
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs973990491
MyVariant Identifiers: chr11:g.2193205T>C (hg19) chr11:g.2171975T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171975T>C , CM000673.2:g.2171975T>C GRCh38
NC_000011.9:g.2193205T>C , CM000673.1:g.2193205T>C GRCh37
NC_000011.8:g.2149781T>C NCBI36
NG_008128.1:g.4831A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-189A>G XP_011518637.1:n.-189A>G
XM_011520335.2:c.-189A>G XP_011518637.1:n.-189A>G
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