Canonical Allele Identifier: CA505124944
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6714050G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6714039G>A , CM000681.2:g.6714039G>A GRCh38
NC_000019.9:g.6714050G>A , CM000681.1:g.6714050G>A GRCh37
NC_000019.8:g.6665050G>A NCBI36
NG_009557.1:g.11613C>T , LRG_27:g.11613C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.603C>T ENSP00000512083.1:p.Phe201=
ENST00000245907.11:c.726C>T MANE Select ENSP00000245907.4:p.Phe242=
ENST00000245907.10:c.726C>T ENSP00000245907.4:p.Phe242=
ENST00000595577.1:n.230C>T
NM_000064.3:c.726C>T NP_000055.2:p.Phe242=
NM_000064.4:c.726C>T MANE Select NP_000055.2:p.Phe242=