Canonical Allele Identifier: CA403643690
Gene: C3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714443G>C , CM000681.2:g.6714443G>C GRCh38
NC_000019.9:g.6714454G>C , CM000681.1:g.6714454G>C GRCh37
NC_000019.8:g.6665454G>C NCBI36
NG_009557.1:g.11209C>G , LRG_27:g.11209C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.385C>G ENSP00000512083.1:p.Pro129Ala
ENST00000245907.11:c.508C>G MANE Select ENSP00000245907.4:p.Pro170Ala
ENST00000245907.10:c.508C>G ENSP00000245907.4:p.Pro170Ala
NM_000064.3:c.508C>G NP_000055.2:p.Pro170Ala
NM_000064.4:c.508C>G MANE Select NP_000055.2:p.Pro170Ala