Canonical Allele Identifier: CA1995884720
Gene: TRPC6 HGNC NCBI

Linked Data

dbSNP Id: rs1858792531

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101452774G>A , CM000673.2:g.101452774G>A GRCh38
NC_000011.9:g.101323505G>A , CM000673.1:g.101323505G>A GRCh37
NC_000011.8:g.100828715G>A NCBI36
NG_011476.1:g.136155C>T
NG_011476.2:g.136155C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344327.8:c.*181C>T MANE Select ENSP00000340913.3:n.*181C>T
ENST00000344327.7:c.*181C>T ENSP00000340913.3:n.*181C>T
NM_004621.5:c.*181C>T NP_004612.2:n.*181C>T
XM_006718898.2:c.*181C>T XP_006718961.1:n.*181C>T
XM_011542968.1:c.*181C>T XP_011541270.1:n.*181C>T
XM_011542968.3:c.*181C>T XP_011541270.1:n.*181C>T
XM_017018221.2:c.*181C>T XP_016873710.1:n.*181C>T
XR_001747948.2:n.3334C>T
NM_004621.6:c.*181C>T MANE Select NP_004612.2:n.*181C>T