Canonical Allele Identifier: CA851782943
Gene: SFRP1 HGNC NCBI

Linked Data

dbSNP Id: rs3242
gnomAD v3: 8-41262035-G-C
gnomAD v4: 8-41262035-G-C
MyVariant Identifiers: chr8:g.41119554G>C (hg19) chr8:g.41262035G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.41262035G>C , CM000670.2:g.41262035G>C GRCh38
NC_000008.10:g.41119554G>C , CM000670.1:g.41119554G>C GRCh37
NC_000008.9:g.41238711G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000220772.8:c.*3132C>G MANE Select ENSP00000220772.3:n.*3132C>G
ENST00000220772.7:c.*3132C>G ENSP00000220772.3:n.*3132C>G
ENST00000379845.3:c.*3132C>G ENSP00000369174.3:n.*3132C>G
NM_003012.4:c.*3132C>G NP_003003.3:n.*3132C>G
NM_003012.5:c.*3132C>G MANE Select NP_003003.3:n.*3132C>G
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