Canonical Allele Identifier: CA1619362437

Gene: C2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31915902C>A , CM000668.2:g.31915902C>A	GRCh38
NC_000006.11:g.31883679C>A , CM000668.1:g.31883679C>A	GRCh37
NC_000006.10:g.31991658C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000452323.7:c.73+14763C>A	ENSP00000392322.2:n.73+14763C>A
ENST00000497706.6:c.-63-17708C>A	ENSP00000417482.2:n.-63-17708C>A
ENST00000695637.1:c.-359-12053C>A	ENSP00000512074.1:n.-359-12053C>A
ENST00000452202.5:c.73+14763C>A	ENSP00000406121.1:n.73+14763C>A
ENST00000452323.6:c.73+14763C>A	ENSP00000392322.2:n.73+14763C>A
ENST00000469372.5:c.-63-17708C>A	ENSP00000418923.1:n.-63-17708C>A
ENST00000497706.5:c.-63-17708C>A	ENSP00000417482.1:n.-63-17708C>A
NM_001178063.2:c.73+14763C>A	NP_001171534.1:n.73+14763C>A
NM_001282457.1:c.-63-17708C>A	NP_001269386.1:n.-63-17708C>A
NM_001282457.2:c.-63-17708C>A	NP_001269386.1:n.-63-17708C>A
NM_001178063.3:c.73+14763C>A	NP_001171534.1:n.73+14763C>A