Canonical Allele Identifier: CA403639234
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6709724T>C (hg19) chr19:g.6709713T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6709713T>C , CM000681.2:g.6709713T>C GRCh38
NC_000019.9:g.6709724T>C , CM000681.1:g.6709724T>C GRCh37
NC_000019.8:g.6660724T>C NCBI36
NG_009557.1:g.15939A>G , LRG_27:g.15939A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.1693A>G ENSP00000512083.1:p.Asn565Asp
ENST00000695654.1:c.940A>G ENSP00000512085.1:p.Asn314Asp
ENST00000695655.1:c.757A>G ENSP00000512086.1:n.757A>G
ENST00000695692.1:n.1180A>G
ENST00000245907.11:c.1816A>G MANE Select ENSP00000245907.4:p.Asn606Asp
ENST00000245907.10:c.1816A>G ENSP00000245907.4:p.Asn606Asp
NM_000064.3:c.1816A>G NP_000055.2:p.Asn606Asp
NM_000064.4:c.1816A>G MANE Select NP_000055.2:p.Asn606Asp
Search 100 bp 5'
Search 100 bp 3'