Canonical Allele Identifier: CA505125059
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6714440C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714429C>G , CM000681.2:g.6714429C>G GRCh38
NC_000019.9:g.6714440C>G , CM000681.1:g.6714440C>G GRCh37
NC_000019.8:g.6665440C>G NCBI36
NG_009557.1:g.11223G>C , LRG_27:g.11223G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.399G>C ENSP00000512083.1:p.Pro133=
ENST00000245907.11:c.522G>C MANE Select ENSP00000245907.4:p.Pro174=
ENST00000245907.10:c.522G>C ENSP00000245907.4:p.Pro174=
NM_000064.3:c.522G>C NP_000055.2:p.Pro174=
NM_000064.4:c.522G>C MANE Select NP_000055.2:p.Pro174=
Search 100 bp 5'
Search 100 bp 3'