Canonical Allele Identifier: CA403643362
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714365G>T , CM000681.2:g.6714365G>T GRCh38
NC_000019.9:g.6714376G>T , CM000681.1:g.6714376G>T GRCh37
NC_000019.8:g.6665376G>T NCBI36
NG_009557.1:g.11287C>A , LRG_27:g.11287C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.463C>A ENSP00000512083.1:p.Pro155Thr
ENST00000245907.11:c.586C>A MANE Select ENSP00000245907.4:p.Pro196Thr
ENST00000245907.10:c.586C>A ENSP00000245907.4:p.Pro196Thr
NM_000064.3:c.586C>A NP_000055.2:p.Pro196Thr
NM_000064.4:c.586C>A MANE Select NP_000055.2:p.Pro196Thr