Canonical Allele Identifier: CA304797836
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs374736261
MyVariant Identifiers: chr19:g.6713386G>T (hg19) chr19:g.6713375G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713375G>T , CM000681.2:g.6713375G>T GRCh38
NC_000019.9:g.6713386G>T , CM000681.1:g.6713386G>T GRCh37
NC_000019.8:g.6664386G>T NCBI36
NG_009557.1:g.12277C>A , LRG_27:g.12277C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.753+32C>A ENSP00000512083.1:n.753+32C>A
ENST00000695692.1:n.200+32C>A
ENST00000245907.11:c.876+32C>A MANE Select ENSP00000245907.4:n.876+32C>A
ENST00000245907.10:c.876+32C>A ENSP00000245907.4:n.876+32C>A
ENST00000595577.1:n.380+32C>A
ENST00000597442.5:n.126+32C>A
NM_000064.3:c.876+32C>A NP_000055.2:n.876+32C>A
NM_000064.4:c.876+32C>A MANE Select NP_000055.2:n.876+32C>A
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