Canonical Allele Identifier: CA884128525

Gene: C3

Linked Data

• dbSNP Id: rs2277982
• gnomAD v4: 19-6679634-C-G
• MyVariant Identifiers: chr19:g.6679645C>G (hg19) ; chr19:g.6679634C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679634C>G , CM000681.2:g.6679634C>G	GRCh38
NC_000019.9:g.6679645C>G , CM000681.1:g.6679645C>G	GRCh37
NC_000019.8:g.6630645C>G	NCBI36
NG_009557.1:g.46018G>C , LRG_27:g.46018G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2805-138G>C
ENST00000695653.1:c.2366-138G>C	ENSP00000512084.1:n.2366-138G>C
ENST00000695654.1:c.3482-138G>C	ENSP00000512085.1:n.3482-138G>C
ENST00000695689.1:c.428-138G>C	ENSP00000512101.1:n.428-138G>C
ENST00000695690.1:n.1522-138G>C
ENST00000695691.1:n.1318-138G>C
ENST00000245907.11:c.4457-138G>C MANE Select	ENSP00000245907.4:n.4457-138G>C
ENST00000245907.10:c.4457-138G>C	ENSP00000245907.4:n.4457-138G>C
ENST00000599668.1:n.52-138G>C
ENST00000599899.5:n.1416-138G>C
ENST00000601008.1:c.242-1676G>C	ENSP00000471384.1:n.242-1676G>C
NM_000064.3:c.4457-138G>C	NP_000055.2:n.4457-138G>C
NM_000064.4:c.4457-138G>C MANE Select	NP_000055.2:n.4457-138G>C