Canonical Allele Identifier: CA403642602

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6713464T>G (hg19) ; chr19:g.6713453T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713453T>G , CM000681.2:g.6713453T>G	GRCh38
NC_000019.9:g.6713464T>G , CM000681.1:g.6713464T>G	GRCh37
NC_000019.8:g.6664464T>G	NCBI36
NG_009557.1:g.12199A>C , LRG_27:g.12199A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.707A>C	ENSP00000512083.1:p.Asp236Ala
ENST00000695692.1:n.154A>C
ENST00000245907.11:c.830A>C MANE Select	ENSP00000245907.4:p.Asp277Ala
ENST00000245907.10:c.830A>C	ENSP00000245907.4:p.Asp277Ala
ENST00000595577.1:n.334A>C
ENST00000597442.5:n.80A>C
NM_000064.3:c.830A>C	NP_000055.2:p.Asp277Ala
NM_000064.4:c.830A>C MANE Select	NP_000055.2:p.Asp277Ala