Canonical Allele Identifier: CA403643465
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6714408T>G (hg19) chr19:g.6714397T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714397T>G , CM000681.2:g.6714397T>G GRCh38
NC_000019.9:g.6714408T>G , CM000681.1:g.6714408T>G GRCh37
NC_000019.8:g.6665408T>G NCBI36
NG_009557.1:g.11255A>C , LRG_27:g.11255A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.431A>C ENSP00000512083.1:p.Gln144Pro
ENST00000245907.11:c.554A>C MANE Select ENSP00000245907.4:p.Gln185Pro
ENST00000245907.10:c.554A>C ENSP00000245907.4:p.Gln185Pro
NM_000064.3:c.554A>C NP_000055.2:p.Gln185Pro
NM_000064.4:c.554A>C MANE Select NP_000055.2:p.Gln185Pro
Search 100 bp 5'
Search 100 bp 3'