Canonical Allele Identifier: CA403642351
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6713319T>C (hg19) chr19:g.6713308T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713308T>C , CM000681.2:g.6713308T>C GRCh38
NC_000019.9:g.6713319T>C , CM000681.1:g.6713319T>C GRCh37
NC_000019.8:g.6664319T>C NCBI36
NG_009557.1:g.12344A>G , LRG_27:g.12344A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.761A>G ENSP00000512083.1:p.Asp254Gly
ENST00000695654.1:c.8A>G ENSP00000512085.1:p.Asp3Gly
ENST00000695692.1:n.208A>G
ENST00000245907.11:c.884A>G MANE Select ENSP00000245907.4:p.Asp295Gly
ENST00000245907.10:c.884A>G ENSP00000245907.4:p.Asp295Gly
ENST00000594270.5:n.8A>G
ENST00000595577.1:n.388A>G
ENST00000597442.5:n.134A>G
NM_000064.3:c.884A>G NP_000055.2:p.Asp295Gly
NM_000064.4:c.884A>G MANE Select NP_000055.2:p.Asp295Gly
Search 100 bp 5'
Search 100 bp 3'