Canonical Allele Identifier: CA304786403

Gene: C3

Linked Data

• dbSNP Id: rs866540490
• gnomAD v2: 19-6697835-T-A
• gnomAD v4: 19-6697824-T-A
• MyVariant Identifiers: chr19:g.6697835T>A (hg19) ; chr19:g.6697824T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697824T>A , CM000681.2:g.6697824T>A	GRCh38
NC_000019.9:g.6697835T>A , CM000681.1:g.6697835T>A	GRCh37
NC_000019.8:g.6648835T>A	NCBI36
NG_009557.1:g.27828A>T , LRG_27:g.27828A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.789-30A>T
ENST00000695652.1:c.2318-30A>T	ENSP00000512083.1:n.2318-30A>T
ENST00000695653.1:c.350-30A>T	ENSP00000512084.1:n.350-30A>T
ENST00000695654.1:c.1565-30A>T	ENSP00000512085.1:n.1565-30A>T
ENST00000695655.1:c.1382-30A>T	ENSP00000512086.1:n.1382-30A>T
ENST00000695692.1:n.1805-30A>T
ENST00000245907.11:c.2441-30A>T MANE Select	ENSP00000245907.4:n.2441-30A>T
ENST00000245907.10:c.2441-30A>T	ENSP00000245907.4:n.2441-30A>T
ENST00000602053.1:n.489-30A>T
NM_000064.3:c.2441-30A>T	NP_000055.2:n.2441-30A>T
NM_000064.4:c.2441-30A>T MANE Select	NP_000055.2:n.2441-30A>T