Canonical Allele Identifier: CA403642961
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6714042A>T (hg19) chr19:g.6714031A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714031A>T , CM000681.2:g.6714031A>T GRCh38
NC_000019.9:g.6714042A>T , CM000681.1:g.6714042A>T GRCh37
NC_000019.8:g.6665042A>T NCBI36
NG_009557.1:g.11621T>A , LRG_27:g.11621T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.611T>A ENSP00000512083.1:p.Ile204Asn
ENST00000245907.11:c.734T>A MANE Select ENSP00000245907.4:p.Ile245Asn
ENST00000245907.10:c.734T>A ENSP00000245907.4:p.Ile245Asn
ENST00000595577.1:n.238T>A
NM_000064.3:c.734T>A NP_000055.2:p.Ile245Asn
NM_000064.4:c.734T>A MANE Select NP_000055.2:p.Ile245Asn
Search 100 bp 5'
Search 100 bp 3'