Canonical Allele Identifier: CA403633985

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6697739G>T (hg19) ; chr19:g.6697728G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6697728G>T , CM000681.2:g.6697728G>T	GRCh38
NC_000019.9:g.6697739G>T , CM000681.1:g.6697739G>T	GRCh37
NC_000019.8:g.6648739G>T	NCBI36
NG_009557.1:g.27924C>A , LRG_27:g.27924C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695651.1:n.855C>A
ENST00000695652.1:c.2384C>A	ENSP00000512083.1:p.Pro795His
ENST00000695653.1:c.416C>A	ENSP00000512084.1:p.Pro139His
ENST00000695654.1:c.1631C>A	ENSP00000512085.1:p.Pro544His
ENST00000695655.1:c.1448C>A	ENSP00000512086.1:n.1448C>A
ENST00000695692.1:n.1871C>A
ENST00000245907.11:c.2507C>A MANE Select	ENSP00000245907.4:p.Pro836His
ENST00000245907.10:c.2507C>A	ENSP00000245907.4:p.Pro836His
ENST00000602053.1:n.555C>A
NM_000064.3:c.2507C>A	NP_000055.2:p.Pro836His
NM_000064.4:c.2507C>A MANE Select	NP_000055.2:p.Pro836His