Canonical Allele Identifier: CA2838210396

Gene: SNTG2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.1099155A>G , CM000664.2:g.1099155A>G	GRCh38
NC_000002.11:g.1094841A>G , CM000664.1:g.1094841A>G	GRCh37
NC_000002.10:g.1084841A>G	NCBI36
NG_029707.1:g.153288A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308624.10:c.325+745A>G MANE Select	ENSP00000311837.5:n.325+745A>G
ENST00000308624.9:c.325+745A>G	ENSP00000311837.5:n.325+745A>G
ENST00000407292.1:c.210+15500A>G	ENSP00000385020.1:n.210+15500A>G
ENST00000450962.5:c.325+745A>G	ENSP00000401997.1:n.325+745A>G
ENST00000452177.5:c.325+745A>G	ENSP00000412249.1:n.325+745A>G
NM_018968.3:c.325+745A>G	NP_061841.2:n.325+745A>G
XM_011510364.1:c.328+745A>G	XP_011508666.1:n.328+745A>G
XM_011510365.1:c.148+745A>G	XP_011508667.1:n.148+745A>G
XM_011510366.1:c.-15+15500A>G	XP_011508668.1:n.-15+15500A>G
XM_011510367.1:c.-53+745A>G	XP_011508669.1:n.-53+745A>G
XM_011510366.2:c.-15+15500A>G	XP_011508668.1:n.-15+15500A>G
XM_017004361.1:c.328+745A>G	XP_016859850.1:n.328+745A>G
XM_017004362.1:c.328+745A>G	XP_016859851.1:n.328+745A>G
XM_017004363.1:c.148+745A>G	XP_016859852.1:n.148+745A>G
XM_017004365.1:c.328+745A>G	XP_016859854.1:n.328+745A>G
XM_017004366.1:c.328+745A>G	XP_016859855.1:n.328+745A>G
XM_017004367.1:c.-53+745A>G	XP_016859856.1:n.-53+745A>G
XM_017004368.1:c.328+745A>G	XP_016859857.1:n.328+745A>G
XM_017004369.1:c.328+745A>G	XP_016859858.1:n.328+745A>G
XM_017004370.1:c.328+745A>G	XP_016859859.1:n.328+745A>G
XM_017004371.1:c.328+745A>G	XP_016859860.1:n.328+745A>G
XM_017004372.1:c.328+745A>G	XP_016859861.1:n.328+745A>G
XM_017004374.1:c.328+745A>G	XP_016859863.1:n.328+745A>G
NM_018968.4:c.325+745A>G MANE Select	NP_061841.2:n.325+745A>G