Canonical Allele Identifier: CA403645221

Gene: C3

Linked Data

• MyVariant Identifiers: chr19:g.6718353C>A (hg19) ; chr19:g.6718342C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6718342C>A , CM000681.2:g.6718342C>A	GRCh38
NC_000019.9:g.6718353C>A , CM000681.1:g.6718353C>A	GRCh37
NC_000019.8:g.6669353C>A	NCBI36
NG_009557.1:g.7310G>T , LRG_27:g.7310G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000594936.2:n.399G>T
ENST00000695652.1:c.215G>T	ENSP00000512083.1:p.Gly72Val
ENST00000695693.1:c.338G>T	ENSP00000512104.1:p.Gly113Val
ENST00000245907.11:c.338G>T MANE Select	ENSP00000245907.4:p.Gly113Val
ENST00000245907.10:c.338G>T	ENSP00000245907.4:p.Gly113Val
ENST00000594936.1:n.399G>T
ENST00000600744.1:c.215G>T	ENSP00000472044.1:p.Gly72Val
NM_000064.3:c.338G>T	NP_000055.2:p.Gly113Val
NM_000064.4:c.338G>T MANE Select	NP_000055.2:p.Gly113Val