Canonical Allele Identifier: CA1619369857
Gene: C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31933783C= , CM000668.2:g.31933783C= GRCh38
NC_000006.11:g.31901560C= , CM000668.1:g.31901560C= GRCh37
NC_000006.10:g.32009539C= NCBI36
NG_011730.1:g.11295C= , LRG_26:g.11295C=

Transcript Alleles

HGVS Amino-acid change
ENST00000447952.7:c.430C= ENSP00000391354.3:p.Gln144=
ENST00000452323.7:c.247C= ENSP00000392322.2:p.Gln83=
ENST00000468407.2:c.616C= ENSP00000512075.1:p.Gln206=
ENST00000497706.6:c.111C= ENSP00000417482.2:p.Ala37=
ENST00000695637.1:c.211C= ENSP00000512074.1:p.Gln71=
ENST00000695638.1:c.616C= ENSP00000512076.1:p.Gln206=
ENST00000695639.1:n.336C=
ENST00000695640.1:n.471C=
ENST00000695644.1:c.220C= ENSP00000512079.1:p.Gln74=
ENST00000299367.10:c.616C= MANE Select ENSP00000299367.5:p.Gln206=
ENST00000299367.9:c.616C= ENSP00000299367.5:p.Gln206=
ENST00000383177.7:c.210C=
ENST00000411571.6:c.111C= ENSP00000388727.2:p.Ala37=
ENST00000418949.6:c.616C= ENSP00000406190.2:p.Gln206=
ENST00000442278.6:c.220C= ENSP00000395683.2:p.Gln74=
ENST00000447952.6:c.430C= ENSP00000391354.2:p.Gln144=
ENST00000452202.5:c.247C= ENSP00000406121.1:p.Gln83=
ENST00000452323.6:c.247C= ENSP00000392322.2:p.Gln83=
ENST00000456570.5:c.430C= ENSP00000410815.1:p.Gln144=
ENST00000469372.5:c.111C= ENSP00000418923.1:p.Ala37=
ENST00000477310.1:c.443-3536C= ENSP00000418996.1:n.443-3536C=
ENST00000482060.5:c.*329C= ENSP00000418332.1:n.*329C=
ENST00000484636.1:c.111C= ENSP00000420305.1:p.Ala37=
ENST00000494905.1:c.193C= ENSP00000419048.1:p.Gln65=
ENST00000497706.5:c.111C= ENSP00000417482.1:p.Ala37=
NM_000063.5:c.616C= NP_000054.2:p.Gln206=
NM_001145903.2:c.220C= NP_001139375.1:p.Gln74=
NM_001178063.2:c.247C= NP_001171534.1:p.Gln83=
NM_001282457.1:c.111C= NP_001269386.1:p.Ala37=
NM_001282458.1:c.529C= NP_001269387.1:p.Gln177=
NM_001282459.1:c.616C= NP_001269388.1:p.Gln206=
NM_000063.6:c.616C= MANE Select NP_000054.2:p.Gln206=
NM_001145903.3:c.220C= NP_001139375.1:p.Gln74=
NM_001282457.2:c.111C= NP_001269386.1:p.Ala37=
NM_001282458.2:c.529C= NP_001269387.1:p.Gln177=
NM_001282459.2:c.616C= NP_001269388.1:p.Gln206=
NM_001178063.3:c.247C= NP_001171534.1:p.Gln83=