Canonical Allele Identifier: CA2611971254

Gene: TH

Linked Data

• gnomAD v4: 11-2165118-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2165118T>C , CM000673.2:g.2165118T>C	GRCh38
NC_000011.9:g.2186348T>C , CM000673.1:g.2186348T>C	GRCh37
NC_000011.8:g.2142924T>C	NCBI36
NG_007114.1:g.1077A>G
NG_008128.1:g.11688A>G
NG_050578.1:g.1092A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.1334+114A>G MANE Select	ENSP00000325951.4:n.1334+114A>G
ENST00000333684.9:c.1052+114A>G	ENSP00000328814.6:n.1052+114A>G
ENST00000352909.7:c.1334+114A>G	ENSP00000325951.3:n.1334+114A>G
ENST00000381175.5:c.1415+114A>G	ENSP00000370567.1:n.1415+114A>G
ENST00000381178.5:c.1427+114A>G	ENSP00000370571.1:n.1427+114A>G
NM_000360.3:c.1334+114A>G	NP_000351.2:n.1334+114A>G
NM_199292.2:c.1427+114A>G	NP_954986.2:n.1427+114A>G
NM_199293.2:c.1415+114A>G	NP_954987.2:n.1415+114A>G
XM_011520335.1:c.1346+114A>G	XP_011518637.1:n.1346+114A>G
XM_011520335.2:c.1346+114A>G	XP_011518637.1:n.1346+114A>G
NM_000360.4:c.1334+114A>G MANE Select	NP_000351.2:n.1334+114A>G
NM_199292.3:c.1427+114A>G	NP_954986.2:n.1427+114A>G
NM_199293.3:c.1415+114A>G	NP_954987.2:n.1415+114A>G