Canonical Allele Identifier: CA216285008

Gene: TH

Linked Data

• dbSNP Id: rs961681928
• gnomAD v4: 11-2166707-G-T
• MyVariant Identifiers: chr11:g.2187937G>T (hg19) ; chr11:g.2166707G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166707G>T , CM000673.2:g.2166707G>T	GRCh38
NC_000011.9:g.2187937G>T , CM000673.1:g.2187937G>T	GRCh37
NC_000011.8:g.2144513G>T	NCBI36
NG_008128.1:g.10099C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.903C>A MANE Select	ENSP00000325951.4:p.Ala301=
ENST00000324155.8:c.*592C>A	ENSP00000325831.3:n.*592C>A
ENST00000333684.9:c.696-158C>A	ENSP00000328814.6:n.696-158C>A
ENST00000352909.7:c.903C>A	ENSP00000325951.3:p.Ala301=
ENST00000381168.7:c.*623C>A	ENSP00000370560.3:n.*623C>A
ENST00000381175.5:c.984C>A	ENSP00000370567.1:p.Ala328=
ENST00000381178.5:c.996C>A	ENSP00000370571.1:p.Ala332=
ENST00000412076.1:c.136-158C>A
ENST00000416223.5:c.197C>A
ENST00000461172.1:n.68C>A
ENST00000479437.5:n.452C>A
NM_000360.3:c.903C>A	NP_000351.2:p.Ala301=
NM_199292.2:c.996C>A	NP_954986.2:p.Ala332=
NM_199293.2:c.984C>A	NP_954987.2:p.Ala328=
XM_011520335.1:c.915C>A	XP_011518637.1:p.Ala305=
XM_011520335.2:c.915C>A	XP_011518637.1:p.Ala305=
NM_000360.4:c.903C>A MANE Select	NP_000351.2:p.Ala301=
NM_199292.3:c.996C>A	NP_954986.2:p.Ala332=
NM_199293.3:c.984C>A	NP_954987.2:p.Ala328=