Canonical Allele Identifier: CA9129721
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs774712170
gnomAD v2: 19-6714127-T-A
gnomAD v4: 19-6714116-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714116T>A , CM000681.2:g.6714116T>A GRCh38
NC_000019.9:g.6714127T>A , CM000681.1:g.6714127T>A GRCh37
NC_000019.8:g.6665127T>A NCBI36
NG_009557.1:g.11536A>T , LRG_27:g.11536A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.560-34A>T ENSP00000512083.1:n.560-34A>T
ENST00000245907.11:c.683-34A>T MANE Select ENSP00000245907.4:n.683-34A>T
ENST00000245907.10:c.683-34A>T ENSP00000245907.4:n.683-34A>T
ENST00000595577.1:n.187-34A>T
NM_000064.3:c.683-34A>T NP_000055.2:n.683-34A>T
NM_000064.4:c.683-34A>T MANE Select NP_000055.2:n.683-34A>T