Canonical Allele Identifier: CA304798369
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs201283596
MyVariant Identifiers: chr19:g.6713883_6713884insT (hg19) chr19:g.6713872_6713873insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6713872_6713873insT , CM000681.2:g.6713872_6713873insT GRCh38
NC_000019.9:g.6713883_6713884insT , CM000681.1:g.6713883_6713884insT GRCh37
NC_000019.8:g.6664883_6664884insT NCBI36
NG_009557.1:g.11779_11780insA , LRG_27:g.11779_11780insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000695652.1:c.650+119_650+120insA ENSP00000512083.1:n.650+119_650+120insA
ENST00000245907.11:c.773+119_773+120insA MANE Select ENSP00000245907.4:n.773+119_773+120insA
ENST00000245907.10:c.773+119_773+120insA ENSP00000245907.4:n.773+119_773+120insA
ENST00000595577.1:n.277+119_277+120insA
NM_000064.3:c.773+119_773+120insA NP_000055.2:n.773+119_773+120insA
NM_000064.4:c.773+119_773+120insA MANE Select NP_000055.2:n.773+119_773+120insA
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