Canonical Allele Identifier: CA403618653

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685146C>A (hg19) ; chr19:g.6685135C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685135C>A , CM000681.2:g.6685135C>A	GRCh38
NC_000019.9:g.6685146C>A , CM000681.1:g.6685146C>A	GRCh37
NC_000019.8:g.6636146C>A	NCBI36
NG_009557.1:g.40517G>T , LRG_27:g.40517G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2170G>T
ENST00000695653.1:c.1731G>T	ENSP00000512084.1:p.Met577Ile
ENST00000695654.1:c.2847G>T	ENSP00000512085.1:p.Met949Ile
ENST00000695690.1:n.13G>T
ENST00000695691.1:n.13G>T
ENST00000245907.11:c.3822G>T MANE Select	ENSP00000245907.4:p.Met1274Ile
ENST00000245907.10:c.3822G>T	ENSP00000245907.4:p.Met1274Ile
ENST00000596238.1:n.265G>T
ENST00000601008.1:c.241+1611G>T	ENSP00000471384.1:n.241+1611G>T
NM_000064.3:c.3822G>T	NP_000055.2:p.Met1274Ile
NM_000064.4:c.3822G>T MANE Select	NP_000055.2:p.Met1274Ile