Canonical Allele Identifier: CA363497016

Gene: C2

Linked Data

• MyVariant Identifiers: chr6:g.31901652T>C (hg19) ; chr6:g.31933875T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31933875T>C , CM000668.2:g.31933875T>C	GRCh38
NC_000006.11:g.31901652T>C , CM000668.1:g.31901652T>C	GRCh37
NC_000006.10:g.32009631T>C	NCBI36
NG_011730.1:g.11387T>C , LRG_26:g.11387T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000447952.7:c.439T>C	ENSP00000391354.3:p.Ser147Pro
ENST00000452323.7:c.256T>C	ENSP00000392322.2:p.Ser86Pro
ENST00000468407.2:c.625T>C	ENSP00000512075.1:p.Ser209Pro
ENST00000497706.6:c.120T>C	ENSP00000417482.2:p.Thr40=
ENST00000695637.1:c.220T>C	ENSP00000512074.1:p.Ser74Pro
ENST00000695638.1:c.625T>C	ENSP00000512076.1:p.Ser209Pro
ENST00000695639.1:n.428T>C
ENST00000695640.1:n.563T>C
ENST00000695644.1:c.229T>C	ENSP00000512079.1:p.Ser77Pro
ENST00000299367.10:c.625T>C MANE Select	ENSP00000299367.5:p.Ser209Pro
ENST00000299367.9:c.625T>C	ENSP00000299367.5:p.Ser209Pro
ENST00000383177.7:c.219T>C
ENST00000411571.6:c.120T>C	ENSP00000388727.2:p.Thr40=
ENST00000418949.6:c.625T>C	ENSP00000406190.2:p.Ser209Pro
ENST00000442278.6:c.229T>C	ENSP00000395683.2:p.Ser77Pro
ENST00000447952.6:c.439T>C	ENSP00000391354.2:p.Ser147Pro
ENST00000452202.5:c.256T>C	ENSP00000406121.1:p.Ser86Pro
ENST00000452323.6:c.256T>C	ENSP00000392322.2:p.Ser86Pro
ENST00000456570.5:c.439T>C	ENSP00000410815.1:p.Ser147Pro
ENST00000469372.5:c.111+92T>C	ENSP00000418923.1:n.111+92T>C
ENST00000477310.1:c.443-3444T>C	ENSP00000418996.1:n.443-3444T>C
ENST00000482060.5:c.*338T>C	ENSP00000418332.1:n.*338T>C
ENST00000484636.1:c.120T>C	ENSP00000420305.1:p.Thr40=
ENST00000494905.1:c.202T>C	ENSP00000419048.1:p.Ser68Pro
ENST00000497706.5:c.120T>C	ENSP00000417482.1:p.Thr40=
NM_000063.5:c.625T>C	NP_000054.2:p.Ser209Pro
NM_001145903.2:c.229T>C	NP_001139375.1:p.Ser77Pro
NM_001178063.2:c.256T>C	NP_001171534.1:p.Ser86Pro
NM_001282457.1:c.111+92T>C	NP_001269386.1:n.111+92T>C
NM_001282458.1:c.538T>C	NP_001269387.1:p.Ser180Pro
NM_001282459.1:c.625T>C	NP_001269388.1:p.Ser209Pro
NM_000063.6:c.625T>C MANE Select	NP_000054.2:p.Ser209Pro
NM_001145903.3:c.229T>C	NP_001139375.1:p.Ser77Pro
NM_001282457.2:c.111+92T>C	NP_001269386.1:n.111+92T>C
NM_001282458.2:c.538T>C	NP_001269387.1:p.Ser180Pro
NM_001282459.2:c.625T>C	NP_001269388.1:p.Ser209Pro
NM_001178063.3:c.256T>C	NP_001171534.1:p.Ser86Pro