Canonical Allele Identifier: CA2320565802
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1967858426
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709514C>A , CM000681.2:g.6709514C>A GRCh38
NC_000019.9:g.6709525C>A , CM000681.1:g.6709525C>A GRCh37
NC_000019.8:g.6660525C>A NCBI36
NG_009557.1:g.16138G>T , LRG_27:g.16138G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1722+170G>T ENSP00000512083.1:n.1722+170G>T
ENST00000695654.1:c.969+170G>T ENSP00000512085.1:n.969+170G>T
ENST00000695655.1:c.786+170G>T ENSP00000512086.1:n.786+170G>T
ENST00000695692.1:n.1209+170G>T
ENST00000245907.11:c.1845+170G>T MANE Select ENSP00000245907.4:n.1845+170G>T
ENST00000245907.10:c.1845+170G>T ENSP00000245907.4:n.1845+170G>T
NM_000064.3:c.1845+170G>T NP_000055.2:n.1845+170G>T
NM_000064.4:c.1845+170G>T MANE Select NP_000055.2:n.1845+170G>T
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