Canonical Allele Identifier: CA403615316

Gene: C3

Linked Data

• gnomAD v4: 19-6682165-G-C
• MyVariant Identifiers: chr19:g.6682176G>C (hg19) ; chr19:g.6682165G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682165G>C , CM000681.2:g.6682165G>C	GRCh38
NC_000019.9:g.6682176G>C , CM000681.1:g.6682176G>C	GRCh37
NC_000019.8:g.6633176G>C	NCBI36
NG_009557.1:g.43487C>G , LRG_27:g.43487C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2585C>G
ENST00000695653.1:c.2146C>G	ENSP00000512084.1:p.Pro716Ala
ENST00000695654.1:c.3262C>G	ENSP00000512085.1:p.Pro1088Ala
ENST00000695689.1:c.208C>G	ENSP00000512101.1:n.208C>G
ENST00000695690.1:n.428C>G
ENST00000695691.1:n.428C>G
ENST00000245907.11:c.4237C>G MANE Select	ENSP00000245907.4:p.Pro1413Ala
ENST00000245907.10:c.4237C>G	ENSP00000245907.4:p.Pro1413Ala
ENST00000596548.1:c.358C>G	ENSP00000469744.1:p.Pro120Ala
ENST00000599899.5:n.1196C>G
ENST00000601008.1:c.242-4207C>G	ENSP00000471384.1:n.242-4207C>G
NM_000064.3:c.4237C>G	NP_000055.2:p.Pro1413Ala
NM_000064.4:c.4237C>G MANE Select	NP_000055.2:p.Pro1413Ala