Canonical Allele Identifier: CA505192529
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6697730-T-C
MyVariant Identifiers: chr19:g.6697741T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6697730T>C , CM000681.2:g.6697730T>C GRCh38
NC_000019.9:g.6697741T>C , CM000681.1:g.6697741T>C GRCh37
NC_000019.8:g.6648741T>C NCBI36
NG_009557.1:g.27922A>G , LRG_27:g.27922A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.853A>G
ENST00000695652.1:c.2382A>G ENSP00000512083.1:p.Leu794=
ENST00000695653.1:c.414A>G ENSP00000512084.1:p.Leu138=
ENST00000695654.1:c.1629A>G ENSP00000512085.1:p.Leu543=
ENST00000695655.1:c.1446A>G ENSP00000512086.1:n.1446A>G
ENST00000695692.1:n.1869A>G
ENST00000245907.11:c.2505A>G MANE Select ENSP00000245907.4:p.Leu835=
ENST00000245907.10:c.2505A>G ENSP00000245907.4:p.Leu835=
ENST00000602053.1:n.553A>G
NM_000064.3:c.2505A>G NP_000055.2:p.Leu835=
NM_000064.4:c.2505A>G MANE Select NP_000055.2:p.Leu835=