Canonical Allele Identifier: CA884131920
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1217228908
MyVariant Identifiers: chr19:g.6685932A>T (hg19) chr19:g.6685921A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6685921A>T , CM000681.2:g.6685921A>T GRCh38
NC_000019.9:g.6685932A>T , CM000681.1:g.6685932A>T GRCh37
NC_000019.8:g.6636932A>T NCBI36
NG_009557.1:g.39731T>A , LRG_27:g.39731T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695651.1:n.2158+203T>A
ENST00000695653.1:c.1719+203T>A ENSP00000512084.1:n.1719+203T>A
ENST00000695654.1:c.2835+203T>A ENSP00000512085.1:n.2835+203T>A
ENST00000245907.11:c.3810+203T>A MANE Select ENSP00000245907.4:n.3810+203T>A
ENST00000245907.10:c.3810+203T>A ENSP00000245907.4:n.3810+203T>A
ENST00000596238.1:n.253+203T>A
ENST00000601008.1:c.241+825T>A ENSP00000471384.1:n.241+825T>A
NM_000064.3:c.3810+203T>A NP_000055.2:n.3810+203T>A
NM_000064.4:c.3810+203T>A MANE Select NP_000055.2:n.3810+203T>A
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