Canonical Allele Identifier: CA2320568193
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1599525268
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713797C>T , CM000681.2:g.6713797C>T GRCh38
NC_000019.9:g.6713808C>T , CM000681.1:g.6713808C>T GRCh37
NC_000019.8:g.6664808C>T NCBI36
NG_009557.1:g.11855G>A , LRG_27:g.11855G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+195G>A ENSP00000512083.1:n.650+195G>A
ENST00000245907.11:c.773+195G>A MANE Select ENSP00000245907.4:n.773+195G>A
ENST00000245907.10:c.773+195G>A ENSP00000245907.4:n.773+195G>A
ENST00000595577.1:n.277+195G>A
NM_000064.3:c.773+195G>A NP_000055.2:n.773+195G>A
NM_000064.4:c.773+195G>A MANE Select NP_000055.2:n.773+195G>A
Search 100 bp 5'
Search 100 bp 3'