Canonical Allele Identifier: CA10581541
Gene: TRPC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 236169
ClinVar RCV Id: RCV000225030
dbSNP Id: rs878853196
MyVariant Identifiers: chr11:g.101353656A>G (hg19) chr11:g.101482925A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101482925A>G , CM000673.2:g.101482925A>G GRCh38
NC_000011.9:g.101353656A>G , CM000673.1:g.101353656A>G GRCh37
NC_000011.8:g.100858866A>G NCBI36
NG_011476.1:g.106004T>C
NG_011476.2:g.106004T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000344327.8:c.1510+24T>C MANE Select ENSP00000340913.3:n.1510+24T>C
ENST00000344327.7:c.1510+24T>C ENSP00000340913.3:n.1510+24T>C
ENST00000348423.8:c.1162+24T>C ENSP00000343672.4:n.1162+24T>C
ENST00000360497.4:c.1345+24T>C ENSP00000353687.4:n.1345+24T>C
ENST00000532133.5:c.1510+24T>C ENSP00000435574.1:n.1510+24T>C
NM_004621.5:c.1510+24T>C NP_004612.2:n.1510+24T>C
XM_006718898.2:c.1510+24T>C XP_006718961.1:n.1510+24T>C
XM_011542968.1:c.1345+24T>C XP_011541270.1:n.1345+24T>C
XM_011542969.1:c.1510+24T>C XP_011541271.1:n.1510+24T>C
XM_011542968.3:c.1345+24T>C XP_011541270.1:n.1345+24T>C
XM_017018221.2:c.1162+24T>C XP_016873710.1:n.1162+24T>C
XR_001747948.2:n.1866+24T>C
NM_004621.6:c.1510+24T>C MANE Select NP_004612.2:n.1510+24T>C
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