Canonical Allele Identifier: CA403618348

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685041G>C (hg19) ; chr19:g.6685030G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685030G>C , CM000681.2:g.6685030G>C	GRCh38
NC_000019.9:g.6685041G>C , CM000681.1:g.6685041G>C	GRCh37
NC_000019.8:g.6636041G>C	NCBI36
NG_009557.1:g.40622C>G , LRG_27:g.40622C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2275C>G
ENST00000695653.1:c.1836C>G	ENSP00000512084.1:p.His612Gln
ENST00000695654.1:c.2952C>G	ENSP00000512085.1:p.His984Gln
ENST00000695690.1:n.118C>G
ENST00000695691.1:n.118C>G
ENST00000245907.11:c.3927C>G MANE Select	ENSP00000245907.4:p.His1309Gln
ENST00000245907.10:c.3927C>G	ENSP00000245907.4:p.His1309Gln
ENST00000596238.1:n.370C>G
ENST00000596548.1:c.9C>G	ENSP00000469744.1:p.His3Gln
ENST00000601008.1:c.241+1716C>G	ENSP00000471384.1:n.241+1716C>G
NM_000064.3:c.3927C>G	NP_000055.2:p.His1309Gln
NM_000064.4:c.3927C>G MANE Select	NP_000055.2:p.His1309Gln