Canonical Allele Identifier: CA346168894

Gene: GTF3C2

Linked Data

• MyVariant Identifiers: chr2:g.27550980A>C (hg19) ; chr2:g.27328113A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27328113A>C , CM000664.2:g.27328113A>C	GRCh38
NC_000002.11:g.27550980A>C , CM000664.1:g.27550980A>C	GRCh37
NC_000002.10:g.27404484A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000264720.8:c.2333T>G MANE Select	ENSP00000264720.3:p.Val778Gly
ENST00000264720.7:c.2333T>G	ENSP00000264720.3:p.Val778Gly
ENST00000359541.6:c.2333T>G	ENSP00000352536.2:p.Val778Gly
ENST00000415683.2:c.600T>G
ENST00000454704.5:c.859T>G
ENST00000457098.5:c.213T>G
ENST00000495298.1:n.378T>G
NM_001035521.2:c.2333T>G	NP_001030598.1:p.Val778Gly
NM_001521.3:c.2333T>G	NP_001512.1:p.Val778Gly
XM_005264272.3:c.2450T>G	XP_005264329.1:p.Val817Gly
XM_005264273.2:c.2366T>G	XP_005264330.1:p.Val789Gly
XM_011532801.1:c.2678T>G	XP_011531103.1:p.Val893Gly
XM_011532802.1:c.2333T>G	XP_011531104.1:p.Val778Gly
NM_001318909.1:c.2366T>G	NP_001305838.1:p.Val789Gly
XM_005264272.5:c.2450T>G	XP_005264329.1:p.Val817Gly
NM_001035521.3:c.2333T>G MANE Select	NP_001030598.1:p.Val778Gly
NM_001318909.2:c.2366T>G	NP_001305838.1:p.Val789Gly
NM_001388380.1:c.2450T>G	NP_001375309.1:p.Val817Gly
NM_001521.4:c.2333T>G	NP_001512.1:p.Val778Gly
NM_001318909.4:c.2333T>G	NP_001305838.2:p.Val778Gly
NM_001388380.3:c.2333T>G	NP_001375309.2:p.Val778Gly
NM_001394503.1:c.2333T>G	NP_001381432.1:p.Val778Gly
NM_001394504.1:c.2333T>G	NP_001381433.1:p.Val778Gly
NM_001394505.1:c.2333T>G	NP_001381434.1:p.Val778Gly
NM_001394506.1:c.2333T>G	NP_001381435.1:p.Val778Gly
NM_001394507.1:c.2333T>G	NP_001381436.1:p.Val778Gly
NM_001394508.1:c.2333T>G	NP_001381437.1:p.Val778Gly
NM_001394509.1:c.2333T>G	NP_001381438.1:p.Val778Gly
NM_001394510.1:c.2333T>G	NP_001381439.1:p.Val778Gly
NM_001394511.1:c.2333T>G	NP_001381440.1:p.Val778Gly
NM_001394512.1:c.2321T>G	NP_001381441.1:p.Val774Gly
NM_001394514.1:c.2255T>G	NP_001381443.1:p.Val752Gly
NM_001394515.1:c.2177T>G	NP_001381444.1:p.Val726Gly
NM_001394516.1:c.2105T>G	NP_001381445.1:p.Val702Gly