Canonical Allele Identifier: CA884148722

Gene: C3

Linked Data

• dbSNP Id: rs1305025309
• gnomAD v3: 19-6710005-G-A
• gnomAD v4: 19-6710005-G-A
• MyVariant Identifiers: chr19:g.6710016G>A (hg19) ; chr19:g.6710005G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6710005G>A , CM000681.2:g.6710005G>A	GRCh38
NC_000019.9:g.6710016G>A , CM000681.1:g.6710016G>A	GRCh37
NC_000019.8:g.6661016G>A	NCBI36
NG_009557.1:g.15647C>T , LRG_27:g.15647C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.1564-163C>T	ENSP00000512083.1:n.1564-163C>T
ENST00000695654.1:c.811-163C>T	ENSP00000512085.1:n.811-163C>T
ENST00000695655.1:c.592-127C>T	ENSP00000512086.1:n.592-127C>T
ENST00000695692.1:n.1051-163C>T
ENST00000245907.11:c.1687-163C>T MANE Select	ENSP00000245907.4:n.1687-163C>T
ENST00000245907.10:c.1687-163C>T	ENSP00000245907.4:n.1687-163C>T
ENST00000600763.1:n.320-163C>T
NM_000064.3:c.1687-163C>T	NP_000055.2:n.1687-163C>T
NM_000064.4:c.1687-163C>T MANE Select	NP_000055.2:n.1687-163C>T