Canonical Allele Identifier: CA2320553005
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs2241393
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6685293G>T , CM000681.2:g.6685293G>T GRCh38
NC_000019.9:g.6685304G>T , CM000681.1:g.6685304G>T GRCh37
NC_000019.8:g.6636304G>T NCBI36
NG_009557.1:g.40359C>A , LRG_27:g.40359C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2159-147C>A
ENST00000695653.1:c.1720-147C>A ENSP00000512084.1:n.1720-147C>A
ENST00000695654.1:c.2836-147C>A ENSP00000512085.1:n.2836-147C>A
ENST00000245907.11:c.3811-147C>A MANE Select ENSP00000245907.4:n.3811-147C>A
ENST00000245907.10:c.3811-147C>A ENSP00000245907.4:n.3811-147C>A
ENST00000596238.1:n.254-147C>A
ENST00000601008.1:c.241+1453C>A ENSP00000471384.1:n.241+1453C>A
NM_000064.3:c.3811-147C>A NP_000055.2:n.3811-147C>A
NM_000064.4:c.3811-147C>A MANE Select NP_000055.2:n.3811-147C>A
Search 100 bp 5'
Search 100 bp 3'