Canonical Allele Identifier: CA176282344
Gene: SFRP1 HGNC NCBI

Linked Data

dbSNP Id: rs767852789
MyVariant Identifiers: chr8:g.41119854A>G (hg19) chr8:g.41262335A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41262335A>G , CM000670.2:g.41262335A>G GRCh38
NC_000008.10:g.41119854A>G , CM000670.1:g.41119854A>G GRCh37
NC_000008.9:g.41239011A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220772.8:c.*2832T>C MANE Select ENSP00000220772.3:n.*2832T>C
ENST00000220772.7:c.*2832T>C ENSP00000220772.3:n.*2832T>C
ENST00000379845.3:c.*2832T>C ENSP00000369174.3:n.*2832T>C
NM_003012.4:c.*2832T>C NP_003003.3:n.*2832T>C
NM_003012.5:c.*2832T>C MANE Select NP_003003.3:n.*2832T>C
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