Canonical Allele Identifier: CA691438892

Gene: C1R

Linked Data

• dbSNP Id: rs1367032910
• gnomAD v3: 12-7086264-G-C
• gnomAD v4: 12-7086264-G-C
• MyVariant Identifiers: chr12:g.7086264G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086264G>C , CM000674.2:g.7086264G>C	GRCh38
NG_062465.1:g.11344C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.1117+115C>G MANE Select	ENSP00000497341.1:n.1117+115C>G
ENST00000648162.1:n.1089+115C>G
ENST00000649804.1:c.211+115C>G	ENSP00000497938.1:n.211+115C>G
ENST00000535233.6:c.1015+115C>G	ENSP00000438636.3:n.1015+115C>G
ENST00000536053.6:c.1159+115C>G	ENSP00000444271.3:n.1159+115C>G
ENST00000540394.5:n.2182+115C>G
ENST00000542285.5:c.1117+115C>G	ENSP00000438615.2:n.1117+115C>G
ENST00000602298.2:n.1466+115C>G
NM_001733.4:c.1117+115C>G	NP_001724.3:n.1117+115C>G
NM_001354346.1:c.1159+115C>G	NP_001341275.1:n.1159+115C>G
NM_001733.6:c.1117+115C>G	NP_001724.4:n.1117+115C>G
NM_001733.7:c.1117+115C>G MANE Select	NP_001724.4:n.1117+115C>G
NM_001354346.2:c.1159+115C>G	NP_001341275.1:n.1159+115C>G