Canonical Allele Identifier: CA691438957

Gene: C1R

Linked Data

• dbSNP Id: rs1352879804
• gnomAD v3: 12-7086330-G-A
• gnomAD v4: 12-7086330-G-A
• MyVariant Identifiers: chr12:g.7086330G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7086330G>A , CM000674.2:g.7086330G>A	GRCh38
NG_062465.1:g.11278C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647956.2:c.1117+49C>T MANE Select	ENSP00000497341.1:n.1117+49C>T
ENST00000648162.1:n.1089+49C>T
ENST00000649804.1:c.211+49C>T	ENSP00000497938.1:n.211+49C>T
ENST00000535233.6:c.1015+49C>T	ENSP00000438636.3:n.1015+49C>T
ENST00000536053.6:c.1159+49C>T	ENSP00000444271.3:n.1159+49C>T
ENST00000540394.5:n.2182+49C>T
ENST00000542285.5:c.1117+49C>T	ENSP00000438615.2:n.1117+49C>T
ENST00000602298.2:n.1466+49C>T
NM_001733.4:c.1117+49C>T	NP_001724.3:n.1117+49C>T
NM_001354346.1:c.1159+49C>T	NP_001341275.1:n.1159+49C>T
NM_001733.6:c.1117+49C>T	NP_001724.4:n.1117+49C>T
NM_001733.7:c.1117+49C>T MANE Select	NP_001724.4:n.1117+49C>T
NM_001354346.2:c.1159+49C>T	NP_001341275.1:n.1159+49C>T