Canonical Allele Identifier: CA505122527

Gene: C3

Linked Data

• dbSNP Id: rs1309924953
• gnomAD v2: 19-6682871-A-T
• gnomAD v3: 19-6682860-A-T
• gnomAD v4: 19-6682860-A-T
• MyVariant Identifiers: chr19:g.6682871A>T (hg19) ; chr19:g.6682860A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6682860A>T , CM000681.2:g.6682860A>T	GRCh38
NC_000019.9:g.6682871A>T , CM000681.1:g.6682871A>T	GRCh37
NC_000019.8:g.6633871A>T	NCBI36
NG_009557.1:g.42792T>A , LRG_27:g.42792T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.2521-631T>A
ENST00000695653.1:c.2082-631T>A	ENSP00000512084.1:n.2082-631T>A
ENST00000695654.1:c.3198-631T>A	ENSP00000512085.1:n.3198-631T>A
ENST00000695689.1:c.84-194T>A	ENSP00000512101.1:n.84-194T>A
ENST00000695690.1:n.364-631T>A
ENST00000695691.1:n.364-631T>A
ENST00000245907.11:c.4173-631T>A MANE Select	ENSP00000245907.4:n.4173-631T>A
ENST00000245907.10:c.4173-631T>A	ENSP00000245907.4:n.4173-631T>A
ENST00000596548.1:c.294-631T>A	ENSP00000469744.1:n.294-631T>A
ENST00000599899.5:n.501T>A
ENST00000601008.1:c.241+3886T>A	ENSP00000471384.1:n.241+3886T>A
NM_000064.3:c.4173-631T>A	NP_000055.2:n.4173-631T>A
NM_000064.4:c.4173-631T>A MANE Select	NP_000055.2:n.4173-631T>A