Canonical Allele Identifier: CA304797934

Gene: C3

Linked Data

• dbSNP Id: rs112912973
• MyVariant Identifiers: chr19:g.6713415T>A (hg19) ; chr19:g.6713404T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713404T>A , CM000681.2:g.6713404T>A	GRCh38
NC_000019.9:g.6713415T>A , CM000681.1:g.6713415T>A	GRCh37
NC_000019.8:g.6664415T>A	NCBI36
NG_009557.1:g.12248A>T , LRG_27:g.12248A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.753+3A>T	ENSP00000512083.1:n.753+3A>T
ENST00000695692.1:n.200+3A>T
ENST00000245907.11:c.876+3A>T MANE Select	ENSP00000245907.4:n.876+3A>T
ENST00000245907.10:c.876+3A>T	ENSP00000245907.4:n.876+3A>T
ENST00000595577.1:n.380+3A>T
ENST00000597442.5:n.126+3A>T
NM_000064.3:c.876+3A>T	NP_000055.2:n.876+3A>T
NM_000064.4:c.876+3A>T MANE Select	NP_000055.2:n.876+3A>T