Canonical Allele Identifier: CA2587872725

Gene: C3

Linked Data

• gnomAD v4: 19-6682955-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682955G>T , CM000681.2:g.6682955G>T	GRCh38
NC_000019.9:g.6682966G>T , CM000681.1:g.6682966G>T	GRCh37
NC_000019.8:g.6633966G>T	NCBI36
NG_009557.1:g.42697C>A , LRG_27:g.42697C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2521-726C>A
ENST00000695653.1:c.2082-726C>A	ENSP00000512084.1:n.2082-726C>A
ENST00000695654.1:c.3198-726C>A	ENSP00000512085.1:n.3198-726C>A
ENST00000695689.1:c.84-289C>A	ENSP00000512101.1:n.84-289C>A
ENST00000695690.1:n.364-726C>A
ENST00000695691.1:n.364-726C>A
ENST00000245907.11:c.4173-726C>A MANE Select	ENSP00000245907.4:n.4173-726C>A
ENST00000245907.10:c.4173-726C>A	ENSP00000245907.4:n.4173-726C>A
ENST00000596548.1:c.294-726C>A	ENSP00000469744.1:n.294-726C>A
ENST00000599899.5:n.406C>A
ENST00000601008.1:c.241+3791C>A	ENSP00000471384.1:n.241+3791C>A
NM_000064.3:c.4173-726C>A	NP_000055.2:n.4173-726C>A
NM_000064.4:c.4173-726C>A MANE Select	NP_000055.2:n.4173-726C>A