Canonical Allele Identifier: CA884137323
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs163913
MyVariant Identifiers: chr19:g.6722635C>G (hg19) chr19:g.6722624C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6722624C>G , CM000681.2:g.6722624C>G GRCh38
NC_000019.9:g.6722635C>G , CM000681.1:g.6722635C>G GRCh37
NC_000019.8:g.6673635C>G NCBI36
NG_009557.1:g.3028G>C , LRG_27:g.3028G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000600744.1:c.-50+817G>C ENSP00000472044.1:n.-50+817G>C
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