Canonical Allele Identifier: CA359591464

Gene: C7

Linked Data

• MyVariant Identifiers: chr5:g.40964966C>G (hg19) ; chr5:g.40964864C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40964864C>G , CM000667.2:g.40964864C>G	GRCh38
NC_000005.9:g.40964966C>G , CM000667.1:g.40964966C>G	GRCh37
NC_000005.8:g.41000723C>G	NCBI36
NG_011692.1:g.60368C>G , LRG_30:g.60368C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000486779.2:n.665C>G
ENST00000696333.1:c.1873C>G	ENSP00000512566.1:p.His625Asp
ENST00000696441.1:c.1873C>G	ENSP00000512631.1:p.His625Asp
ENST00000706664.1:n.1987C>G
ENST00000706666.1:n.1949C>G
ENST00000706667.1:n.2763C>G
ENST00000706668.1:n.2601C>G
ENST00000313164.10:c.1873C>G MANE Select	ENSP00000322061.9:p.His625Asp
ENST00000313164.9:c.1873C>G	ENSP00000322061.9:p.His625Asp
ENST00000486779.1:n.386C>G
NM_000587.2:c.1873C>G , LRG_30t1:c.1873C>G	NP_000578.2:p.His625Asp
XM_011514122.1:c.1873C>G	XP_011512424.1:p.His625Asp
NM_000587.3:c.1873C>G	NP_000578.2:p.His625Asp
NM_000587.4:c.1873C>G MANE Select	NP_000578.2:p.His625Asp