Canonical Allele Identifier: CA884131907
Gene: C3 HGNC NCBI

Linked Data

dbSNP Id: rs1254619321
MyVariant Identifiers: chr19:g.6685928_6685929del (hg19) chr19:g.6685917_6685918del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6685922_6685923del , CM000681.2:g.6685922_6685923del GRCh38
NC_000019.9:g.6685933_6685934del , CM000681.1:g.6685933_6685934del GRCh37
NC_000019.8:g.6636933_6636934del NCBI36
NG_009557.1:g.39734_39735del , LRG_27:g.39734_39735del

Transcript Alleles

HGVS Amino-acid change
ENST00000695651.1:n.2158+206_2158+207del
ENST00000695653.1:c.1719+206_1719+207del ENSP00000512084.1:n.1719+206_1719+207del
ENST00000695654.1:c.2835+206_2835+207del ENSP00000512085.1:n.2835+206_2835+207del
ENST00000245907.11:c.3810+206_3810+207del MANE Select ENSP00000245907.4:n.3810+206_3810+207del
ENST00000245907.10:c.3810+206_3810+207del ENSP00000245907.4:n.3810+206_3810+207del
ENST00000596238.1:n.253+206_253+207del
ENST00000601008.1:c.241+828_241+829del ENSP00000471384.1:n.241+828_241+829del
NM_000064.3:c.3810+206_3810+207del NP_000055.2:n.3810+206_3810+207del
NM_000064.4:c.3810+206_3810+207del MANE Select NP_000055.2:n.3810+206_3810+207del
Search 100 bp 5'
Search 100 bp 3'