Canonical Allele Identifier: CA2587878774
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6714552-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714552T>C , CM000681.2:g.6714552T>C GRCh38
NC_000019.9:g.6714563T>C , CM000681.1:g.6714563T>C GRCh37
NC_000019.8:g.6665563T>C NCBI36
NG_009557.1:g.11100A>G , LRG_27:g.11100A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.382-106A>G ENSP00000512083.1:n.382-106A>G
ENST00000245907.11:c.505-106A>G MANE Select ENSP00000245907.4:n.505-106A>G
ENST00000245907.10:c.505-106A>G ENSP00000245907.4:n.505-106A>G
NM_000064.3:c.505-106A>G NP_000055.2:n.505-106A>G
NM_000064.4:c.505-106A>G MANE Select NP_000055.2:n.505-106A>G
Search 100 bp 5'
Search 100 bp 3'