Canonical Allele Identifier: CA2576592445
Gene: C3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714270G>T , CM000681.2:g.6714270G>T GRCh38
NC_000019.9:g.6714281G>T , CM000681.1:g.6714281G>T GRCh37
NC_000019.8:g.6665281G>T NCBI36
NG_009557.1:g.11382C>A , LRG_27:g.11382C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.477-22C>A ENSP00000512083.1:n.477-22C>A
ENST00000245907.11:c.600-22C>A MANE Select ENSP00000245907.4:n.600-22C>A
ENST00000245907.10:c.600-22C>A ENSP00000245907.4:n.600-22C>A
ENST00000595577.1:n.82C>A
NM_000064.3:c.600-22C>A NP_000055.2:n.600-22C>A
NM_000064.4:c.600-22C>A MANE Select NP_000055.2:n.600-22C>A