Canonical Allele Identifier: CA176282345
Gene: SFRP1 HGNC NCBI

Linked Data

dbSNP Id: rs995638840
MyVariant Identifiers: chr8:g.41119880G>A (hg19) chr8:g.41262361G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41262361G>A , CM000670.2:g.41262361G>A GRCh38
NC_000008.10:g.41119880G>A , CM000670.1:g.41119880G>A GRCh37
NC_000008.9:g.41239037G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000220772.8:c.*2806C>T MANE Select ENSP00000220772.3:n.*2806C>T
ENST00000220772.7:c.*2806C>T ENSP00000220772.3:n.*2806C>T
ENST00000379845.3:c.*2806C>T ENSP00000369174.3:n.*2806C>T
NM_003012.4:c.*2806C>T NP_003003.3:n.*2806C>T
NM_003012.5:c.*2806C>T MANE Select NP_003003.3:n.*2806C>T
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