Canonical Allele Identifier: CA2587873366
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6686019-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6686019G>T , CM000681.2:g.6686019G>T GRCh38
NC_000019.9:g.6686030G>T , CM000681.1:g.6686030G>T GRCh37
NC_000019.8:g.6637030G>T NCBI36
NG_009557.1:g.39633C>A , LRG_27:g.39633C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2158+105C>A
ENST00000695653.1:c.1719+105C>A ENSP00000512084.1:n.1719+105C>A
ENST00000695654.1:c.2835+105C>A ENSP00000512085.1:n.2835+105C>A
ENST00000245907.11:c.3810+105C>A MANE Select ENSP00000245907.4:n.3810+105C>A
ENST00000245907.10:c.3810+105C>A ENSP00000245907.4:n.3810+105C>A
ENST00000596238.1:n.253+105C>A
ENST00000601008.1:c.241+727C>A ENSP00000471384.1:n.241+727C>A
NM_000064.3:c.3810+105C>A NP_000055.2:n.3810+105C>A
NM_000064.4:c.3810+105C>A MANE Select NP_000055.2:n.3810+105C>A
Search 100 bp 5'
Search 100 bp 3'