Canonical Allele Identifier: CA505193131

Gene: C3

Linked Data

• gnomAD v4: 19-6713458-G-A
• MyVariant Identifiers: chr19:g.6713469G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713458G>A , CM000681.2:g.6713458G>A	GRCh38
NC_000019.9:g.6713469G>A , CM000681.1:g.6713469G>A	GRCh37
NC_000019.8:g.6664469G>A	NCBI36
NG_009557.1:g.12194C>T , LRG_27:g.12194C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.702C>T	ENSP00000512083.1:p.Ile234=
ENST00000695692.1:n.149C>T
ENST00000245907.11:c.825C>T MANE Select	ENSP00000245907.4:p.Ile275=
ENST00000245907.10:c.825C>T	ENSP00000245907.4:p.Ile275=
ENST00000595577.1:n.329C>T
ENST00000597442.5:n.75C>T
NM_000064.3:c.825C>T	NP_000055.2:p.Ile275=
NM_000064.4:c.825C>T MANE Select	NP_000055.2:p.Ile275=