Canonical Allele Identifier: CA403643228
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6714236G>C (hg19) chr19:g.6714225G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714225G>C , CM000681.2:g.6714225G>C GRCh38
NC_000019.9:g.6714236G>C , CM000681.1:g.6714236G>C GRCh37
NC_000019.8:g.6665236G>C NCBI36
NG_009557.1:g.11427C>G , LRG_27:g.11427C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.500C>G ENSP00000512083.1:p.Ala167Gly
ENST00000245907.11:c.623C>G MANE Select ENSP00000245907.4:p.Ala208Gly
ENST00000245907.10:c.623C>G ENSP00000245907.4:p.Ala208Gly
ENST00000595577.1:n.127C>G
NM_000064.3:c.623C>G NP_000055.2:p.Ala208Gly
NM_000064.4:c.623C>G MANE Select NP_000055.2:p.Ala208Gly
Search 100 bp 5'
Search 100 bp 3'