Canonical Allele Identifier: CA884132005

Gene: C3

Linked Data

• dbSNP Id: rs1348635364
• gnomAD v4: 19-6713947-GGTCCCTCACCTGGCTCTTACCTGGCCCCACCCCCA-G
• MyVariant Identifiers: chr19:g.6713959_6713993del (hg19) ; chr19:g.6713948_6713982del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6713962_6713996del , CM000681.2:g.6713962_6713996del	GRCh38
NC_000019.9:g.6713973_6714007del , CM000681.1:g.6713973_6714007del	GRCh37
NC_000019.8:g.6664973_6665007del	NCBI36
NG_009557.1:g.11670_11704del , LRG_27:g.11670_11704del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695652.1:c.650+10_650+44del
ENST00000245907.11:c.773+10_773+44del
ENST00000245907.10:c.773+10_773+44del
ENST00000595577.1:n.277+10_277+44del
NM_000064.3:c.773+10_773+44del
NM_000064.4:c.773+10_773+44del