Canonical Allele Identifier: CA5818479

Gene: TH

Linked Data

• ClinVar Variation Id: 1098929
• ClinVar RCV Id: RCV001421047
• dbSNP Id: rs776737582
• ExAC: 11:2188136 G / A
• gnomAD v2: 11-2188136-G-A
• gnomAD v4: 11-2166906-G-A
• MyVariant Identifiers: chr11:g.2188136G>A (hg19) ; chr11:g.2166906G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166906G>A , CM000673.2:g.2166906G>A	GRCh38
NC_000011.9:g.2188136G>A , CM000673.1:g.2188136G>A	GRCh37
NC_000011.8:g.2144712G>A	NCBI36
NG_008128.1:g.9900C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.822C>T MANE Select	ENSP00000325951.4:p.Asp274=
ENST00000324155.8:c.*511C>T	ENSP00000325831.3:n.*511C>T
ENST00000333684.9:c.696-357C>T	ENSP00000328814.6:n.696-357C>T
ENST00000352909.7:c.822C>T	ENSP00000325951.3:p.Asp274=
ENST00000381168.7:c.*542C>T	ENSP00000370560.3:n.*542C>T
ENST00000381175.5:c.903C>T	ENSP00000370567.1:p.Asp301=
ENST00000381178.5:c.915C>T	ENSP00000370571.1:p.Asp305=
ENST00000412076.1:c.136-357C>T
ENST00000416223.5:c.136-138C>T
ENST00000469226.1:n.951C>T
ENST00000479437.5:n.371C>T
NM_000360.3:c.822C>T	NP_000351.2:p.Asp274=
NM_199292.2:c.915C>T	NP_954986.2:p.Asp305=
NM_199293.2:c.903C>T	NP_954987.2:p.Asp301=
XM_011520335.1:c.834C>T	XP_011518637.1:p.Asp278=
XM_011520335.2:c.834C>T	XP_011518637.1:p.Asp278=
NM_000360.4:c.822C>T MANE Select	NP_000351.2:p.Asp274=
NM_199292.3:c.915C>T	NP_954986.2:p.Asp305=
NM_199293.3:c.903C>T	NP_954987.2:p.Asp301=