Canonical Allele Identifier: CA1995884726
Gene: TRPC6 HGNC NCBI

Linked Data

dbSNP Id: rs1858792589
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101452779A>T , CM000673.2:g.101452779A>T GRCh38
NC_000011.9:g.101323510A>T , CM000673.1:g.101323510A>T GRCh37
NC_000011.8:g.100828720A>T NCBI36
NG_011476.1:g.136150T>A
NG_011476.2:g.136150T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000344327.8:c.*176T>A MANE Select ENSP00000340913.3:n.*176T>A
ENST00000344327.7:c.*176T>A ENSP00000340913.3:n.*176T>A
NM_004621.5:c.*176T>A NP_004612.2:n.*176T>A
XM_006718898.2:c.*176T>A XP_006718961.1:n.*176T>A
XM_011542968.1:c.*176T>A XP_011541270.1:n.*176T>A
XM_011542968.3:c.*176T>A XP_011541270.1:n.*176T>A
XM_017018221.2:c.*176T>A XP_016873710.1:n.*176T>A
XR_001747948.2:n.3329T>A
NM_004621.6:c.*176T>A MANE Select NP_004612.2:n.*176T>A
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