Canonical Allele Identifier: CA505123595

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6685152G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6685141G>T , CM000681.2:g.6685141G>T	GRCh38
NC_000019.9:g.6685152G>T , CM000681.1:g.6685152G>T	GRCh37
NC_000019.8:g.6636152G>T	NCBI36
NG_009557.1:g.40511C>A , LRG_27:g.40511C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.2164C>A
ENST00000695653.1:c.1725C>A	ENSP00000512084.1:p.Thr575=
ENST00000695654.1:c.2841C>A	ENSP00000512085.1:p.Thr947=
ENST00000695690.1:n.7C>A
ENST00000695691.1:n.7C>A
ENST00000245907.11:c.3816C>A MANE Select	ENSP00000245907.4:p.Thr1272=
ENST00000245907.10:c.3816C>A	ENSP00000245907.4:p.Thr1272=
ENST00000596238.1:n.259C>A
ENST00000601008.1:c.241+1605C>A	ENSP00000471384.1:n.241+1605C>A
NM_000064.3:c.3816C>A	NP_000055.2:p.Thr1272=
NM_000064.4:c.3816C>A MANE Select	NP_000055.2:p.Thr1272=