Canonical Allele Identifier: CA472018847

Gene: TH

Linked Data

• dbSNP Id: rs767080132
• MyVariant Identifiers: chr11:g.2191000G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169770G>T , CM000673.2:g.2169770G>T	GRCh38
NC_000011.9:g.2191000G>T , CM000673.1:g.2191000G>T	GRCh37
NC_000011.8:g.2147576G>T	NCBI36
NG_008128.1:g.7036C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.192C>A MANE Select	ENSP00000325951.4:p.Pro64=
ENST00000324155.8:c.91-75C>A	ENSP00000325831.3:n.91-75C>A
ENST00000333684.9:c.192C>A	ENSP00000328814.6:p.Pro64=
ENST00000352909.7:c.192C>A	ENSP00000325951.3:p.Pro64=
ENST00000381168.7:c.103-75C>A	ENSP00000370560.3:n.103-75C>A
ENST00000381175.5:c.273C>A	ENSP00000370567.1:p.Pro91=
ENST00000381178.5:c.285C>A	ENSP00000370571.1:p.Pro95=
NM_000360.3:c.192C>A	NP_000351.2:p.Pro64=
NM_199292.2:c.285C>A	NP_954986.2:p.Pro95=
NM_199293.2:c.273C>A	NP_954987.2:p.Pro91=
XM_011520335.1:c.204C>A	XP_011518637.1:p.Pro68=
XM_011520335.2:c.204C>A	XP_011518637.1:p.Pro68=
NM_000360.4:c.192C>A MANE Select	NP_000351.2:p.Pro64=
NM_199292.3:c.285C>A	NP_954986.2:p.Pro95=
NM_199293.3:c.273C>A	NP_954987.2:p.Pro91=