Canonical Allele Identifier: CA1619369908
Gene: C2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31933896G= , CM000668.2:g.31933896G= GRCh38
NC_000006.11:g.31901673G= , CM000668.1:g.31901673G= GRCh37
NC_000006.10:g.32009652G= NCBI36
NG_011730.1:g.11408G= , LRG_26:g.11408G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000447952.7:c.460G= ENSP00000391354.3:p.Val154=
ENST00000452323.7:c.277G= ENSP00000392322.2:p.Val93=
ENST00000468407.2:c.646G= ENSP00000512075.1:p.Val216=
ENST00000497706.6:c.141G= ENSP00000417482.2:p.Thr47=
ENST00000695637.1:c.241G= ENSP00000512074.1:p.Val81=
ENST00000695638.1:c.646G= ENSP00000512076.1:p.Val216=
ENST00000695639.1:n.449G=
ENST00000695640.1:n.584G=
ENST00000695644.1:c.250G= ENSP00000512079.1:p.Val84=
ENST00000299367.10:c.646G= MANE Select ENSP00000299367.5:p.Val216=
ENST00000299367.9:c.646G= ENSP00000299367.5:p.Val216=
ENST00000383177.7:c.240G=
ENST00000411571.6:c.141G= ENSP00000388727.2:p.Thr47=
ENST00000418949.6:c.646G= ENSP00000406190.2:p.Val216=
ENST00000442278.6:c.250G= ENSP00000395683.2:p.Val84=
ENST00000447952.6:c.460G= ENSP00000391354.2:p.Val154=
ENST00000452202.5:c.277G= ENSP00000406121.1:p.Val93=
ENST00000452323.6:c.277G= ENSP00000392322.2:p.Val93=
ENST00000456570.5:c.460G= ENSP00000410815.1:p.Val154=
ENST00000469372.5:c.111+113G= ENSP00000418923.1:n.111+113G=
ENST00000477310.1:c.443-3423G= ENSP00000418996.1:n.443-3423G=
ENST00000482060.5:c.*359G= ENSP00000418332.1:n.*359G=
ENST00000484636.1:c.141G= ENSP00000420305.1:p.Thr47=
ENST00000494905.1:c.223G= ENSP00000419048.1:p.Val75=
ENST00000497706.5:c.141G= ENSP00000417482.1:p.Thr47=
NM_000063.5:c.646G= NP_000054.2:p.Val216=
NM_001145903.2:c.250G= NP_001139375.1:p.Val84=
NM_001178063.2:c.277G= NP_001171534.1:p.Val93=
NM_001282457.1:c.111+113G= NP_001269386.1:n.111+113G=
NM_001282458.1:c.559G= NP_001269387.1:p.Val187=
NM_001282459.1:c.646G= NP_001269388.1:p.Val216=
NM_000063.6:c.646G= MANE Select NP_000054.2:p.Val216=
NM_001145903.3:c.250G= NP_001139375.1:p.Val84=
NM_001282457.2:c.111+113G= NP_001269386.1:n.111+113G=
NM_001282458.2:c.559G= NP_001269387.1:p.Val187=
NM_001282459.2:c.646G= NP_001269388.1:p.Val216=
NM_001178063.3:c.277G= NP_001171534.1:p.Val93=