Canonical Allele Identifier: CA403614614

Gene: C3

Linked Data

• dbSNP Id: rs1917874671
• gnomAD v4: 19-6681966-T-C
• MyVariant Identifiers: chr19:g.6681977T>C (hg19) ; chr19:g.6681966T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6681966T>C , CM000681.2:g.6681966T>C	GRCh38
NC_000019.9:g.6681977T>C , CM000681.1:g.6681977T>C	GRCh37
NC_000019.8:g.6632977T>C	NCBI36
NG_009557.1:g.43686A>G , LRG_27:g.43686A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2673A>G
ENST00000695653.1:c.2234A>G	ENSP00000512084.1:p.Asn745Ser
ENST00000695654.1:c.3350A>G	ENSP00000512085.1:p.Asn1117Ser
ENST00000695689.1:c.296A>G	ENSP00000512101.1:n.296A>G
ENST00000695690.1:n.516A>G
ENST00000695691.1:n.516A>G
ENST00000245907.11:c.4325A>G MANE Select	ENSP00000245907.4:p.Asn1442Ser
ENST00000245907.10:c.4325A>G	ENSP00000245907.4:p.Asn1442Ser
ENST00000596548.1:c.446A>G	ENSP00000469744.1:p.Asn149Ser
ENST00000599899.5:n.1284A>G
ENST00000601008.1:c.242-4008A>G	ENSP00000471384.1:n.242-4008A>G
NM_000064.3:c.4325A>G	NP_000055.2:p.Asn1442Ser
NM_000064.4:c.4325A>G MANE Select	NP_000055.2:p.Asn1442Ser