Canonical Allele Identifier: CA1619369849
Gene: C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31933759A= , CM000668.2:g.31933759A= GRCh38
NC_000006.11:g.31901536A= , CM000668.1:g.31901536A= GRCh37
NC_000006.10:g.32009515A= NCBI36
NG_011730.1:g.11271A= , LRG_26:g.11271A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447952.7:c.406A= ENSP00000391354.3:p.Ser136=
ENST00000452323.7:c.223A= ENSP00000392322.2:p.Ser75=
ENST00000468407.2:c.592A= ENSP00000512075.1:p.Ser198=
ENST00000497706.6:c.87A= ENSP00000417482.2:p.Gly29=
ENST00000695637.1:c.187A= ENSP00000512074.1:p.Ser63=
ENST00000695638.1:c.592A= ENSP00000512076.1:p.Ser198=
ENST00000695639.1:n.312A=
ENST00000695640.1:n.447A=
ENST00000695644.1:c.196A= ENSP00000512079.1:p.Ser66=
ENST00000299367.10:c.592A= MANE Select ENSP00000299367.5:p.Ser198=
ENST00000299367.9:c.592A= ENSP00000299367.5:p.Ser198=
ENST00000383177.7:c.186A=
ENST00000411571.6:c.87A= ENSP00000388727.2:p.Gly29=
ENST00000418949.6:c.592A= ENSP00000406190.2:p.Ser198=
ENST00000442278.6:c.196A= ENSP00000395683.2:p.Ser66=
ENST00000447952.6:c.406A= ENSP00000391354.2:p.Ser136=
ENST00000452202.5:c.223A= ENSP00000406121.1:p.Ser75=
ENST00000452323.6:c.223A= ENSP00000392322.2:p.Ser75=
ENST00000456570.5:c.406A= ENSP00000410815.1:p.Ser136=
ENST00000469372.5:c.87A= ENSP00000418923.1:p.Gly29=
ENST00000477310.1:c.443-3560A= ENSP00000418996.1:n.443-3560A=
ENST00000482060.5:c.*305A= ENSP00000418332.1:n.*305A=
ENST00000484636.1:c.87A= ENSP00000420305.1:p.Gly29=
ENST00000494905.1:c.169A= ENSP00000419048.1:p.Ser57=
ENST00000497706.5:c.87A= ENSP00000417482.1:p.Gly29=
NM_000063.5:c.592A= NP_000054.2:p.Ser198=
NM_001145903.2:c.196A= NP_001139375.1:p.Ser66=
NM_001178063.2:c.223A= NP_001171534.1:p.Ser75=
NM_001282457.1:c.87A= NP_001269386.1:p.Gly29=
NM_001282458.1:c.505A= NP_001269387.1:p.Ser169=
NM_001282459.1:c.592A= NP_001269388.1:p.Ser198=
NM_000063.6:c.592A= MANE Select NP_000054.2:p.Ser198=
NM_001145903.3:c.196A= NP_001139375.1:p.Ser66=
NM_001282457.2:c.87A= NP_001269386.1:p.Gly29=
NM_001282458.2:c.505A= NP_001269387.1:p.Ser169=
NM_001282459.2:c.592A= NP_001269388.1:p.Ser198=
NM_001178063.3:c.223A= NP_001171534.1:p.Ser75=