Canonical Allele Identifier: CA304771634

Gene: C3

Linked Data

• dbSNP Id: rs45511693
• gnomAD v4: 19-6679310-C-G
• MyVariant Identifiers: chr19:g.6679310C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6679310C>G , CM000681.2:g.6679310C>G	GRCh38
NC_000019.9:g.6679321C>G , CM000681.1:g.6679321C>G	GRCh37
NC_000019.8:g.6630321C>G	NCBI36
NG_009557.1:g.46342G>C , LRG_27:g.46342G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2894+97G>C
ENST00000695653.1:c.2455+97G>C	ENSP00000512084.1:n.2455+97G>C
ENST00000695654.1:c.3571+97G>C	ENSP00000512085.1:n.3571+97G>C
ENST00000695689.1:c.517+97G>C	ENSP00000512101.1:n.517+97G>C
ENST00000695690.1:n.1611+97G>C
ENST00000695691.1:n.1407+97G>C
ENST00000245907.11:c.4546+97G>C MANE Select	ENSP00000245907.4:n.4546+97G>C
ENST00000245907.10:c.4546+97G>C	ENSP00000245907.4:n.4546+97G>C
ENST00000599668.1:n.166+72G>C
ENST00000599899.5:n.1505+97G>C
ENST00000601008.1:c.242-1352G>C	ENSP00000471384.1:n.242-1352G>C
NM_000064.3:c.4546+97G>C	NP_000055.2:n.4546+97G>C
NM_000064.4:c.4546+97G>C MANE Select	NP_000055.2:n.4546+97G>C