Canonical Allele Identifier: CA403642226

Gene: C3

Linked Data

• gnomAD v4: 19-6713272-A-G
• MyVariant Identifiers: chr19:g.6713283A>G (hg19) ; chr19:g.6713272A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713272A>G , CM000681.2:g.6713272A>G	GRCh38
NC_000019.9:g.6713283A>G , CM000681.1:g.6713283A>G	GRCh37
NC_000019.8:g.6664283A>G	NCBI36
NG_009557.1:g.12380T>C , LRG_27:g.12380T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.797T>C	ENSP00000512083.1:p.Leu266Pro
ENST00000695654.1:c.44T>C	ENSP00000512085.1:p.Leu15Pro
ENST00000695692.1:n.244T>C
ENST00000245907.11:c.920T>C MANE Select	ENSP00000245907.4:p.Leu307Pro
ENST00000245907.10:c.920T>C	ENSP00000245907.4:p.Leu307Pro
ENST00000594270.5:n.44T>C
ENST00000595577.1:n.424T>C
ENST00000597442.5:n.170T>C
NM_000064.3:c.920T>C	NP_000055.2:p.Leu307Pro
NM_000064.4:c.920T>C MANE Select	NP_000055.2:p.Leu307Pro