Canonical Allele Identifier: CA2576592422
Gene: C3 HGNC NCBI

Linked Data

gnomAD v4: 19-6713911-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713911T>A , CM000681.2:g.6713911T>A GRCh38
NC_000019.9:g.6713922T>A , CM000681.1:g.6713922T>A GRCh37
NC_000019.8:g.6664922T>A NCBI36
NG_009557.1:g.11741A>T , LRG_27:g.11741A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+81A>T ENSP00000512083.1:n.650+81A>T
ENST00000245907.11:c.773+81A>T MANE Select ENSP00000245907.4:n.773+81A>T
ENST00000245907.10:c.773+81A>T ENSP00000245907.4:n.773+81A>T
ENST00000595577.1:n.277+81A>T
NM_000064.3:c.773+81A>T NP_000055.2:n.773+81A>T
NM_000064.4:c.773+81A>T MANE Select NP_000055.2:n.773+81A>T
Search 100 bp 5'
Search 100 bp 3'