Canonical Allele Identifier: CA228235893

Gene: TRPC6

Linked Data

• dbSNP Id: rs201923280
• gnomAD v3: 11-101452773-T-C
• gnomAD v4: 11-101452773-T-C
• MyVariant Identifiers: chr11:g.101323504T>C (hg19) ; chr11:g.101452773T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.101452773T>C , CM000673.2:g.101452773T>C	GRCh38
NC_000011.9:g.101323504T>C , CM000673.1:g.101323504T>C	GRCh37
NC_000011.8:g.100828714T>C	NCBI36
NG_011476.1:g.136156A>G
NG_011476.2:g.136156A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000344327.8:c.*182A>G MANE Select	ENSP00000340913.3:n.*182A>G
ENST00000344327.7:c.*182A>G	ENSP00000340913.3:n.*182A>G
NM_004621.5:c.*182A>G	NP_004612.2:n.*182A>G
XM_006718898.2:c.*182A>G	XP_006718961.1:n.*182A>G
XM_011542968.1:c.*182A>G	XP_011541270.1:n.*182A>G
XM_011542968.3:c.*182A>G	XP_011541270.1:n.*182A>G
XM_017018221.2:c.*182A>G	XP_016873710.1:n.*182A>G
XR_001747948.2:n.3335A>G
NM_004621.6:c.*182A>G MANE Select	NP_004612.2:n.*182A>G