Canonical Allele Identifier: CA473394603

Gene: GTF2H1

Linked Data

• dbSNP Id: rs1865016228
• gnomAD v3: 11-18335920-A-G
• gnomAD v4: 11-18335920-A-G
• MyVariant Identifiers: chr11:g.18357467A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18335920A>G , CM000673.2:g.18335920A>G	GRCh38
NC_000011.9:g.18357467A>G , CM000673.1:g.18357467A>G	GRCh37
NC_000011.8:g.18314043A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.321A>G MANE Select	ENSP00000265963.4:p.Ala107=
ENST00000265963.8:c.321A>G	ENSP00000265963.4:p.Ala107=
ENST00000418116.6:n.520A>G
ENST00000453096.6:c.321A>G	ENSP00000393638.2:p.Ala107=
ENST00000534641.5:c.-1-2189A>G	ENSP00000435375.1:n.-1-2189A>G
ENST00000543932.5:n.734A>G
NM_001142307.1:c.321A>G	NP_001135779.1:p.Ala107=
NM_005316.3:c.321A>G	NP_005307.1:p.Ala107=
XM_006718208.2:c.321A>G	XP_006718271.1:p.Ala107=
XM_006718208.3:c.321A>G	XP_006718271.1:p.Ala107=
XM_024448457.1:c.321A>G	XP_024304225.1:p.Ala107=
XM_024448458.1:c.321A>G	XP_024304226.1:p.Ala107=
NM_005316.4:c.321A>G MANE Select	NP_005307.1:p.Ala107=
NM_001142307.2:c.321A>G	NP_001135779.1:p.Ala107=