Canonical Allele Identifier: CA851783071
Gene: SFRP1 HGNC NCBI

Linked Data

dbSNP Id: rs1327620717
MyVariant Identifiers: chr8:g.41119864C>T (hg19) chr8:g.41262345C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41262345C>T , CM000670.2:g.41262345C>T GRCh38
NC_000008.10:g.41119864C>T , CM000670.1:g.41119864C>T GRCh37
NC_000008.9:g.41239021C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220772.8:c.*2822G>A MANE Select ENSP00000220772.3:n.*2822G>A
ENST00000220772.7:c.*2822G>A ENSP00000220772.3:n.*2822G>A
ENST00000379845.3:c.*2822G>A ENSP00000369174.3:n.*2822G>A
NM_003012.4:c.*2822G>A NP_003003.3:n.*2822G>A
NM_003012.5:c.*2822G>A MANE Select NP_003003.3:n.*2822G>A
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