Canonical Allele Identifier: CA10581528
Gene: TRPC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 236155
ClinVar RCV Id: RCV000225044
dbSNP Id: rs878853183
MyVariant Identifiers: chr11:g.101324354G>C (hg19) chr11:g.101453623G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101453623G>C , CM000673.2:g.101453623G>C GRCh38
NC_000011.9:g.101324354G>C , CM000673.1:g.101324354G>C GRCh37
NC_000011.8:g.100829564G>C NCBI36
NG_011476.1:g.135306C>G
NG_011476.2:g.135306C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000344327.8:c.2644+27C>G MANE Select ENSP00000340913.3:n.2644+27C>G
ENST00000344327.7:c.2644+27C>G ENSP00000340913.3:n.2644+27C>G
ENST00000348423.8:c.2296+27C>G ENSP00000343672.4:n.2296+27C>G
ENST00000360497.4:c.2479+27C>G ENSP00000353687.4:n.2479+27C>G
ENST00000532133.5:c.2410+27C>G ENSP00000435574.1:n.2410+27C>G
NM_004621.5:c.2644+27C>G NP_004612.2:n.2644+27C>G
XM_006718898.2:c.2569+27C>G XP_006718961.1:n.2569+27C>G
XM_011542968.1:c.2479+27C>G XP_011541270.1:n.2479+27C>G
XM_011542968.3:c.2479+27C>G XP_011541270.1:n.2479+27C>G
XM_017018221.2:c.2296+27C>G XP_016873710.1:n.2296+27C>G
XR_001747948.2:n.3001+27C>G
NM_004621.6:c.2644+27C>G MANE Select NP_004612.2:n.2644+27C>G
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