Canonical Allele Identifier: CA379112547
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1353124114
gnomAD v2: 11-2191098-G-A
gnomAD v4: 11-2169868-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2169868G>A , CM000673.2:g.2169868G>A GRCh38
NC_000011.9:g.2191098G>A , CM000673.1:g.2191098G>A GRCh37
NC_000011.8:g.2147674G>A NCBI36
NG_008128.1:g.6938C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000352909.8:c.94C>T MANE Select ENSP00000325951.4:p.Pro32Ser
ENST00000324155.8:c.91-173C>T ENSP00000325831.3:n.91-173C>T
ENST00000333684.9:c.94C>T ENSP00000328814.6:p.Pro32Ser
ENST00000352909.7:c.94C>T ENSP00000325951.3:p.Pro32Ser
ENST00000381168.7:c.103-173C>T ENSP00000370560.3:n.103-173C>T
ENST00000381175.5:c.175C>T ENSP00000370567.1:p.Pro59Ser
ENST00000381178.5:c.187C>T ENSP00000370571.1:p.Pro63Ser
NM_000360.3:c.94C>T NP_000351.2:p.Pro32Ser
NM_199292.2:c.187C>T NP_954986.2:p.Pro63Ser
NM_199293.2:c.175C>T NP_954987.2:p.Pro59Ser
XM_011520335.1:c.106C>T XP_011518637.1:p.Pro36Ser
XM_011520335.2:c.106C>T XP_011518637.1:p.Pro36Ser
NM_000360.4:c.94C>T MANE Select NP_000351.2:p.Pro32Ser
NM_199292.3:c.187C>T NP_954986.2:p.Pro63Ser
NM_199293.3:c.175C>T NP_954987.2:p.Pro59Ser