Canonical Allele Identifier: CA403643061
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6714084C>G (hg19) chr19:g.6714073C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714073C>G , CM000681.2:g.6714073C>G GRCh38
NC_000019.9:g.6714084C>G , CM000681.1:g.6714084C>G GRCh37
NC_000019.8:g.6665084C>G NCBI36
NG_009557.1:g.11579G>C , LRG_27:g.11579G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.569G>C ENSP00000512083.1:p.Ser190Thr
ENST00000245907.11:c.692G>C MANE Select ENSP00000245907.4:p.Ser231Thr
ENST00000245907.10:c.692G>C ENSP00000245907.4:p.Ser231Thr
ENST00000595577.1:n.196G>C
NM_000064.3:c.692G>C NP_000055.2:p.Ser231Thr
NM_000064.4:c.692G>C MANE Select NP_000055.2:p.Ser231Thr
Search 100 bp 5'
Search 100 bp 3'