Canonical Allele Identifier: CA379517584

Gene: GTF2H1

Linked Data

• MyVariant Identifiers: chr11:g.18357372A>C (hg19) ; chr11:g.18335825A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18335825A>C , CM000673.2:g.18335825A>C	GRCh38
NC_000011.9:g.18357372A>C , CM000673.1:g.18357372A>C	GRCh37
NC_000011.8:g.18313948A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265963.9:c.226A>C MANE Select	ENSP00000265963.4:p.Asn76His
ENST00000265963.8:c.226A>C	ENSP00000265963.4:p.Asn76His
ENST00000418116.6:n.425A>C
ENST00000453096.6:c.226A>C	ENSP00000393638.2:p.Asn76His
ENST00000525831.5:c.226A>C	ENSP00000431481.1:p.Asn76His
ENST00000531757.5:n.496A>C
ENST00000534641.5:c.-1-2284A>C	ENSP00000435375.1:n.-1-2284A>C
ENST00000543932.5:n.639A>C
NM_001142307.1:c.226A>C	NP_001135779.1:p.Asn76His
NM_005316.3:c.226A>C	NP_005307.1:p.Asn76His
XM_006718208.2:c.226A>C	XP_006718271.1:p.Asn76His
XM_006718208.3:c.226A>C	XP_006718271.1:p.Asn76His
XM_024448457.1:c.226A>C	XP_024304225.1:p.Asn76His
XM_024448458.1:c.226A>C	XP_024304226.1:p.Asn76His
NM_005316.4:c.226A>C MANE Select	NP_005307.1:p.Asn76His
NM_001142307.2:c.226A>C	NP_001135779.1:p.Asn76His