Canonical Allele Identifier: CA1955551768
Gene: GTF2H1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18335968T= , CM000673.2:g.18335968T= GRCh38
NC_000011.9:g.18357515T= , CM000673.1:g.18357515T= GRCh37
NC_000011.8:g.18314091T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265963.9:c.347+22T= MANE Select ENSP00000265963.4:n.347+22T=
ENST00000265963.8:c.347+22T= ENSP00000265963.4:n.347+22T=
ENST00000418116.6:n.546+22T=
ENST00000453096.6:c.347+22T= ENSP00000393638.2:n.347+22T=
ENST00000534641.5:c.-1-2141T= ENSP00000435375.1:n.-1-2141T=
ENST00000543932.5:n.760+22T=
NM_001142307.1:c.347+22T= NP_001135779.1:n.347+22T=
NM_005316.3:c.347+22T= NP_005307.1:n.347+22T=
XM_006718208.2:c.347+22T= XP_006718271.1:n.347+22T=
XM_006718208.3:c.347+22T= XP_006718271.1:n.347+22T=
XM_024448457.1:c.347+22T= XP_024304225.1:n.347+22T=
XM_024448458.1:c.347+22T= XP_024304226.1:n.347+22T=
NM_005316.4:c.347+22T= MANE Select NP_005307.1:n.347+22T=
NM_001142307.2:c.347+22T= NP_001135779.1:n.347+22T=