Canonical Allele Identifier: CA838194298
Gene: SFRP4 HGNC NCBI
EPDR1 HGNC NCBI

Linked Data

dbSNP Id: rs1184760257
gnomAD v3: 7-37906653-A-G
gnomAD v4: 7-37906653-A-G
MyVariant Identifiers: chr7:g.37946255A>G (hg19) chr7:g.37906653A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906653A>G , CM000669.2:g.37906653A>G GRCh38
NC_000007.13:g.37946255A>G , CM000669.1:g.37946255A>G GRCh37
NC_000007.12:g.37912780A>G NCBI36
NG_052980.1:g.15271T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*826T>C (SFRP4) MANE Select ENSP00000410715.2:n.*826T>C
ENST00000436072.6:c.*826T>C (SFRP4) ENSP00000410715.2:n.*826T>C
ENST00000476620.1:c.-37-42187A>G (EPDR1) ENSP00000425858.1:n.-37-42187A>G
NM_003014.3:c.*826T>C (SFRP4) NP_003005.2:n.*826T>C
NM_003014.4:c.*826T>C (SFRP4) MANE Select NP_003005.2:n.*826T>C
Search 100 bp 5'
Search 100 bp 3'