Canonical Allele Identifier: CA403633098

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697491G>T (hg19) ; chr19:g.6697480G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697480G>T , CM000681.2:g.6697480G>T	GRCh38
NC_000019.9:g.6697491G>T , CM000681.1:g.6697491G>T	GRCh37
NC_000019.8:g.6648491G>T	NCBI36
NG_009557.1:g.28172C>A , LRG_27:g.28172C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695651.1:n.1008C>A
ENST00000695652.1:c.2537C>A	ENSP00000512083.1:p.Thr846Asn
ENST00000695653.1:c.569C>A	ENSP00000512084.1:p.Thr190Asn
ENST00000695654.1:c.1784C>A	ENSP00000512085.1:p.Thr595Asn
ENST00000695655.1:c.1601C>A	ENSP00000512086.1:n.1601C>A
ENST00000695692.1:n.2024C>A
ENST00000245907.11:c.2660C>A MANE Select	ENSP00000245907.4:p.Thr887Asn
ENST00000245907.10:c.2660C>A	ENSP00000245907.4:p.Thr887Asn
ENST00000594005.1:n.236C>A
NM_000064.3:c.2660C>A	NP_000055.2:p.Thr887Asn
NM_000064.4:c.2660C>A MANE Select	NP_000055.2:p.Thr887Asn