Canonical Allele Identifier: CA1619357147

Gene: C2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31902478G= , CM000668.2:g.31902478G=	GRCh38
NC_000006.11:g.31870255G= , CM000668.1:g.31870255G=	GRCh37
NC_000006.10:g.31978234G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452323.7:c.73+1339G=	ENSP00000392322.2:n.73+1339G=
ENST00000497706.6:c.-64+4536G=	ENSP00000417482.2:n.-64+4536G=
ENST00000695637.1:c.-360+4203G=	ENSP00000512074.1:n.-360+4203G=
ENST00000452202.5:c.73+1339G=	ENSP00000406121.1:n.73+1339G=
ENST00000452323.6:c.73+1339G=	ENSP00000392322.2:n.73+1339G=
ENST00000469372.5:c.-64+4536G=	ENSP00000418923.1:n.-64+4536G=
ENST00000497706.5:c.-64+4536G=	ENSP00000417482.1:n.-64+4536G=
NM_001178063.2:c.73+1339G=	NP_001171534.1:n.73+1339G=
NM_001282457.1:c.-64+4536G=	NP_001269386.1:n.-64+4536G=
NM_001282457.2:c.-64+4536G=	NP_001269386.1:n.-64+4536G=
NM_001178063.3:c.73+1339G=	NP_001171534.1:n.73+1339G=