Canonical Allele Identifier: CA2582310932
Gene: C3 HGNC NCBI

Linked Data

gnomAD v3: 19-6713918-A-G
gnomAD v4: 19-6713918-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713918A>G , CM000681.2:g.6713918A>G GRCh38
NC_000019.9:g.6713929A>G , CM000681.1:g.6713929A>G GRCh37
NC_000019.8:g.6664929A>G NCBI36
NG_009557.1:g.11734T>C , LRG_27:g.11734T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+74T>C ENSP00000512083.1:n.650+74T>C
ENST00000245907.11:c.773+74T>C MANE Select ENSP00000245907.4:n.773+74T>C
ENST00000245907.10:c.773+74T>C ENSP00000245907.4:n.773+74T>C
ENST00000595577.1:n.277+74T>C
NM_000064.3:c.773+74T>C NP_000055.2:n.773+74T>C
NM_000064.4:c.773+74T>C MANE Select NP_000055.2:n.773+74T>C
Search 100 bp 5'
Search 100 bp 3'