Canonical Allele Identifier: CA363496765
Gene: C2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31933773C>G , CM000668.2:g.31933773C>G GRCh38
NC_000006.11:g.31901550C>G , CM000668.1:g.31901550C>G GRCh37
NC_000006.10:g.32009529C>G NCBI36
NG_011730.1:g.11285C>G , LRG_26:g.11285C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000447952.7:c.420C>G ENSP00000391354.3:p.Pro140=
ENST00000452323.7:c.237C>G ENSP00000392322.2:p.Pro79=
ENST00000468407.2:c.606C>G ENSP00000512075.1:p.Pro202=
ENST00000497706.6:c.101C>G ENSP00000417482.2:p.Pro34Arg
ENST00000695637.1:c.201C>G ENSP00000512074.1:p.Pro67=
ENST00000695638.1:c.606C>G ENSP00000512076.1:p.Pro202=
ENST00000695639.1:n.326C>G
ENST00000695640.1:n.461C>G
ENST00000695644.1:c.210C>G ENSP00000512079.1:p.Pro70=
ENST00000299367.10:c.606C>G MANE Select ENSP00000299367.5:p.Pro202=
ENST00000299367.9:c.606C>G ENSP00000299367.5:p.Pro202=
ENST00000383177.7:c.200C>G
ENST00000411571.6:c.101C>G ENSP00000388727.2:p.Pro34Arg
ENST00000418949.6:c.606C>G ENSP00000406190.2:p.Pro202=
ENST00000442278.6:c.210C>G ENSP00000395683.2:p.Pro70=
ENST00000447952.6:c.420C>G ENSP00000391354.2:p.Pro140=
ENST00000452202.5:c.237C>G ENSP00000406121.1:p.Pro79=
ENST00000452323.6:c.237C>G ENSP00000392322.2:p.Pro79=
ENST00000456570.5:c.420C>G ENSP00000410815.1:p.Pro140=
ENST00000469372.5:c.101C>G ENSP00000418923.1:p.Pro34Arg
ENST00000477310.1:c.443-3546C>G ENSP00000418996.1:n.443-3546C>G
ENST00000482060.5:c.*319C>G ENSP00000418332.1:n.*319C>G
ENST00000484636.1:c.101C>G ENSP00000420305.1:p.Pro34Arg
ENST00000494905.1:c.183C>G ENSP00000419048.1:p.Pro61=
ENST00000497706.5:c.101C>G ENSP00000417482.1:p.Pro34Arg
NM_000063.5:c.606C>G NP_000054.2:p.Pro202=
NM_001145903.2:c.210C>G NP_001139375.1:p.Pro70=
NM_001178063.2:c.237C>G NP_001171534.1:p.Pro79=
NM_001282457.1:c.101C>G NP_001269386.1:p.Pro34Arg
NM_001282458.1:c.519C>G NP_001269387.1:p.Pro173=
NM_001282459.1:c.606C>G NP_001269388.1:p.Pro202=
NM_000063.6:c.606C>G MANE Select NP_000054.2:p.Pro202=
NM_001145903.3:c.210C>G NP_001139375.1:p.Pro70=
NM_001282457.2:c.101C>G NP_001269386.1:p.Pro34Arg
NM_001282458.2:c.519C>G NP_001269387.1:p.Pro173=
NM_001282459.2:c.606C>G NP_001269388.1:p.Pro202=
NM_001178063.3:c.237C>G NP_001171534.1:p.Pro79=