Canonical Allele Identifier: CA631662042

Gene: C3

Linked Data

• dbSNP Id: rs1431279271
• gnomAD v2: 19-6712786-C-T
• gnomAD v3: 19-6712775-C-T
• gnomAD v4: 19-6712775-C-T
• MyVariant Identifiers: chr19:g.6712786C>T (hg19) ; chr19:g.6712775C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6712775C>T , CM000681.2:g.6712775C>T	GRCh38
NC_000019.9:g.6712786C>T , CM000681.1:g.6712786C>T	GRCh37
NC_000019.8:g.6663786C>T	NCBI36
NG_009557.1:g.12877G>A , LRG_27:g.12877G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.881-152G>A	ENSP00000512083.1:n.881-152G>A
ENST00000695654.1:c.128-152G>A	ENSP00000512085.1:n.128-152G>A
ENST00000695692.1:n.328-112G>A
ENST00000245907.11:c.1004-152G>A MANE Select	ENSP00000245907.4:n.1004-152G>A
ENST00000245907.10:c.1004-152G>A	ENSP00000245907.4:n.1004-152G>A
ENST00000594270.5:n.128-173G>A
ENST00000595577.1:n.508-152G>A
ENST00000597442.5:n.254-152G>A
NM_000064.3:c.1004-152G>A	NP_000055.2:n.1004-152G>A
NM_000064.4:c.1004-152G>A MANE Select	NP_000055.2:n.1004-152G>A