Canonical Allele Identifier: CA403619904

Gene: C3

Linked Data

• dbSNP Id: rs1180894540
• gnomAD v3: 19-6686236-G-A
• gnomAD v4: 19-6686236-G-A
• MyVariant Identifiers: chr19:g.6686247G>A (hg19) ; chr19:g.6686236G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6686236G>A , CM000681.2:g.6686236G>A	GRCh38
NC_000019.9:g.6686247G>A , CM000681.1:g.6686247G>A	GRCh37
NC_000019.8:g.6637247G>A	NCBI36
NG_009557.1:g.39416C>T , LRG_27:g.39416C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2046C>T
ENST00000695652.1:c.3575C>T	ENSP00000512083.1:p.Thr1192Ile
ENST00000695653.1:c.1607C>T	ENSP00000512084.1:p.Thr536Ile
ENST00000695654.1:c.2723C>T	ENSP00000512085.1:p.Thr908Ile
ENST00000695655.1:c.2639C>T	ENSP00000512086.1:n.2639C>T
ENST00000695692.1:n.3062C>T
ENST00000245907.11:c.3698C>T MANE Select	ENSP00000245907.4:p.Thr1233Ile
ENST00000245907.10:c.3698C>T	ENSP00000245907.4:p.Thr1233Ile
ENST00000596238.1:n.141C>T
ENST00000601008.1:c.241+510C>T	ENSP00000471384.1:n.241+510C>T
NM_000064.3:c.3698C>T	NP_000055.2:p.Thr1233Ile
NM_000064.4:c.3698C>T MANE Select	NP_000055.2:p.Thr1233Ile