Canonical Allele Identifier: CA157145636
Gene: SFRP4 HGNC NCBI
EPDR1 HGNC NCBI

Linked Data

dbSNP Id: rs762013836
gnomAD v3: 7-37906792-A-G
gnomAD v4: 7-37906792-A-G
MyVariant Identifiers: chr7:g.37946394A>G (hg19) chr7:g.37906792A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906792A>G , CM000669.2:g.37906792A>G GRCh38
NC_000007.13:g.37946394A>G , CM000669.1:g.37946394A>G GRCh37
NC_000007.12:g.37912919A>G NCBI36
NG_052980.1:g.15132T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*687T>C (SFRP4) MANE Select ENSP00000410715.2:n.*687T>C
ENST00000436072.6:c.*687T>C (SFRP4) ENSP00000410715.2:n.*687T>C
ENST00000476620.1:c.-37-42048A>G (EPDR1) ENSP00000425858.1:n.-37-42048A>G
NM_003014.3:c.*687T>C (SFRP4) NP_003005.2:n.*687T>C
NM_003014.4:c.*687T>C (SFRP4) MANE Select NP_003005.2:n.*687T>C
Search 100 bp 5'
Search 100 bp 3'