Canonical Allele Identifier: CA403642392
Gene: C3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.6713328T>A (hg19) chr19:g.6713317T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713317T>A , CM000681.2:g.6713317T>A GRCh38
NC_000019.9:g.6713328T>A , CM000681.1:g.6713328T>A GRCh37
NC_000019.8:g.6664328T>A NCBI36
NG_009557.1:g.12335A>T , LRG_27:g.12335A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.754-2A>T ENSP00000512083.1:n.754-2A>T
ENST00000695692.1:n.201-2A>T
ENST00000245907.11:c.877-2A>T MANE Select ENSP00000245907.4:n.877-2A>T
ENST00000245907.10:c.877-2A>T ENSP00000245907.4:n.877-2A>T
ENST00000595577.1:n.381-2A>T
ENST00000597442.5:n.127-2A>T
NM_000064.3:c.877-2A>T NP_000055.2:n.877-2A>T
NM_000064.4:c.877-2A>T MANE Select NP_000055.2:n.877-2A>T
Search 100 bp 5'
Search 100 bp 3'