Canonical Allele Identifier: CA631722525

Gene: C3

Linked Data

• gnomAD v2: 19-6709646-G-A
• gnomAD v4: 19-6709635-G-A
• MyVariant Identifiers: chr19:g.6709646G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6709635G>A , CM000681.2:g.6709635G>A	GRCh38
NC_000019.9:g.6709646G>A , CM000681.1:g.6709646G>A	GRCh37
NC_000019.8:g.6660646G>A	NCBI36
NG_009557.1:g.16017C>T , LRG_27:g.16017C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695652.1:c.1722+49C>T	ENSP00000512083.1:n.1722+49C>T
ENST00000695654.1:c.969+49C>T	ENSP00000512085.1:n.969+49C>T
ENST00000695655.1:c.786+49C>T	ENSP00000512086.1:n.786+49C>T
ENST00000695692.1:n.1209+49C>T
ENST00000245907.11:c.1845+49C>T MANE Select	ENSP00000245907.4:n.1845+49C>T
ENST00000245907.10:c.1845+49C>T	ENSP00000245907.4:n.1845+49C>T
NM_000064.3:c.1845+49C>T	NP_000055.2:n.1845+49C>T
NM_000064.4:c.1845+49C>T MANE Select	NP_000055.2:n.1845+49C>T