Canonical Allele Identifier: CA304797376
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs963097699
MyVariant Identifiers: chr19:g.6713013C>T (hg19) chr19:g.6713002C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713002C>T , CM000681.2:g.6713002C>T GRCh38
NC_000019.9:g.6713013C>T , CM000681.1:g.6713013C>T GRCh37
NC_000019.8:g.6664013C>T NCBI36
NG_009557.1:g.12650G>A , LRG_27:g.12650G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.880+187G>A ENSP00000512083.1:n.880+187G>A
ENST00000695654.1:c.127+187G>A ENSP00000512085.1:n.127+187G>A
ENST00000695692.1:n.327+187G>A
ENST00000245907.11:c.1003+187G>A MANE Select ENSP00000245907.4:n.1003+187G>A
ENST00000245907.10:c.1003+187G>A ENSP00000245907.4:n.1003+187G>A
ENST00000594270.5:n.127+187G>A
ENST00000595577.1:n.507+187G>A
ENST00000597442.5:n.253+187G>A
NM_000064.3:c.1003+187G>A NP_000055.2:n.1003+187G>A
NM_000064.4:c.1003+187G>A MANE Select NP_000055.2:n.1003+187G>A
Search 100 bp 5'
Search 100 bp 3'