Canonical Allele Identifier: CA176282307
Gene: SFRP1 HGNC NCBI

Linked Data

dbSNP Id: rs991197615

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41262042A>C , CM000670.2:g.41262042A>C GRCh38
NC_000008.10:g.41119561A>C , CM000670.1:g.41119561A>C GRCh37
NC_000008.9:g.41238718A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220772.8:c.*3125T>G MANE Select ENSP00000220772.3:n.*3125T>G
ENST00000220772.7:c.*3125T>G ENSP00000220772.3:n.*3125T>G
ENST00000379845.3:c.*3125T>G ENSP00000369174.3:n.*3125T>G
NM_003012.4:c.*3125T>G NP_003003.3:n.*3125T>G
NM_003012.5:c.*3125T>G MANE Select NP_003003.3:n.*3125T>G