Canonical Allele Identifier: CA379112353

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2191001G>T (hg19) ; chr11:g.2169771G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169771G>T , CM000673.2:g.2169771G>T	GRCh38
NC_000011.9:g.2191001G>T , CM000673.1:g.2191001G>T	GRCh37
NC_000011.8:g.2147577G>T	NCBI36
NG_008128.1:g.7035C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.191C>A MANE Select	ENSP00000325951.4:p.Pro64His
ENST00000324155.8:c.91-76C>A	ENSP00000325831.3:n.91-76C>A
ENST00000333684.9:c.191C>A	ENSP00000328814.6:p.Pro64His
ENST00000352909.7:c.191C>A	ENSP00000325951.3:p.Pro64His
ENST00000381168.7:c.103-76C>A	ENSP00000370560.3:n.103-76C>A
ENST00000381175.5:c.272C>A	ENSP00000370567.1:p.Pro91His
ENST00000381178.5:c.284C>A	ENSP00000370571.1:p.Pro95His
NM_000360.3:c.191C>A	NP_000351.2:p.Pro64His
NM_199292.2:c.284C>A	NP_954986.2:p.Pro95His
NM_199293.2:c.272C>A	NP_954987.2:p.Pro91His
XM_011520335.1:c.203C>A	XP_011518637.1:p.Pro68His
XM_011520335.2:c.203C>A	XP_011518637.1:p.Pro68His
NM_000360.4:c.191C>A MANE Select	NP_000351.2:p.Pro64His
NM_199292.3:c.284C>A	NP_954986.2:p.Pro95His
NM_199293.3:c.272C>A	NP_954987.2:p.Pro91His