Canonical Allele Identifier: CA379112872

Gene: TH

Linked Data

• dbSNP Id: rs933425557
• gnomAD v2: 11-2192985-G-A
• gnomAD v4: 11-2171755-G-A
• MyVariant Identifiers: chr11:g.2192985G>A (hg19) ; chr11:g.2171755G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2171755G>A , CM000673.2:g.2171755G>A	GRCh38
NC_000011.9:g.2192985G>A , CM000673.1:g.2192985G>A	GRCh37
NC_000011.8:g.2149561G>A	NCBI36
NG_008128.1:g.5051C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.32C>T MANE Select	ENSP00000325951.4:p.Ala11Val
ENST00000324155.8:c.32C>T	ENSP00000325831.3:p.Ala11Val
ENST00000333684.9:c.32C>T	ENSP00000328814.6:p.Ala11Val
ENST00000352909.7:c.32C>T	ENSP00000325951.3:p.Ala11Val
ENST00000381168.7:c.32C>T	ENSP00000370560.3:p.Ala11Val
ENST00000381175.5:c.32C>T	ENSP00000370567.1:p.Ala11Val
ENST00000381178.5:c.32C>T	ENSP00000370571.1:p.Ala11Val
NM_000360.3:c.32C>T	NP_000351.2:p.Ala11Val
NM_199292.2:c.32C>T	NP_954986.2:p.Ala11Val
NM_199293.2:c.32C>T	NP_954987.2:p.Ala11Val
XM_011520335.1:c.32C>T	XP_011518637.1:p.Ala11Val
XM_011520335.2:c.32C>T	XP_011518637.1:p.Ala11Val
NM_000360.4:c.32C>T MANE Select	NP_000351.2:p.Ala11Val
NM_199292.3:c.32C>T	NP_954986.2:p.Ala11Val
NM_199293.3:c.32C>T	NP_954987.2:p.Ala11Val