Canonical Allele Identifier: CA2587872649
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6682848-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6682848C>T , CM000681.2:g.6682848C>T GRCh38
NC_000019.9:g.6682859C>T , CM000681.1:g.6682859C>T GRCh37
NC_000019.8:g.6633859C>T NCBI36
NG_009557.1:g.42804G>A , LRG_27:g.42804G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2521-619G>A
ENST00000695653.1:c.2082-619G>A ENSP00000512084.1:n.2082-619G>A
ENST00000695654.1:c.3198-619G>A ENSP00000512085.1:n.3198-619G>A
ENST00000695689.1:c.84-182G>A ENSP00000512101.1:n.84-182G>A
ENST00000695690.1:n.364-619G>A
ENST00000695691.1:n.364-619G>A
ENST00000245907.11:c.4173-619G>A MANE Select ENSP00000245907.4:n.4173-619G>A
ENST00000245907.10:c.4173-619G>A ENSP00000245907.4:n.4173-619G>A
ENST00000596548.1:c.294-619G>A ENSP00000469744.1:n.294-619G>A
ENST00000599899.5:n.513G>A
ENST00000601008.1:c.241+3898G>A ENSP00000471384.1:n.241+3898G>A
NM_000064.3:c.4173-619G>A NP_000055.2:n.4173-619G>A
NM_000064.4:c.4173-619G>A MANE Select NP_000055.2:n.4173-619G>A
Search 100 bp 5'
Search 100 bp 3'