Canonical Allele Identifier: CA403615404

Gene: C3

Linked Data

• gnomAD v4: 19-6682181-C-G
• MyVariant Identifiers: chr19:g.6682192C>G (hg19) ; chr19:g.6682181C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682181C>G , CM000681.2:g.6682181C>G	GRCh38
NC_000019.9:g.6682192C>G , CM000681.1:g.6682192C>G	GRCh37
NC_000019.8:g.6633192C>G	NCBI36
NG_009557.1:g.43471G>C , LRG_27:g.43471G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2569G>C
ENST00000695653.1:c.2130G>C	ENSP00000512084.1:p.Met710Ile
ENST00000695654.1:c.3246G>C	ENSP00000512085.1:p.Met1082Ile
ENST00000695689.1:c.192G>C	ENSP00000512101.1:n.192G>C
ENST00000695690.1:n.412G>C
ENST00000695691.1:n.412G>C
ENST00000245907.11:c.4221G>C MANE Select	ENSP00000245907.4:p.Met1407Ile
ENST00000245907.10:c.4221G>C	ENSP00000245907.4:p.Met1407Ile
ENST00000596548.1:c.342G>C	ENSP00000469744.1:p.Met114Ile
ENST00000599899.5:n.1180G>C
ENST00000601008.1:c.242-4223G>C	ENSP00000471384.1:n.242-4223G>C
NM_000064.3:c.4221G>C	NP_000055.2:p.Met1407Ile
NM_000064.4:c.4221G>C MANE Select	NP_000055.2:p.Met1407Ile