Canonical Allele Identifier: CA157145634
Gene: SFRP4 HGNC NCBI
EPDR1 HGNC NCBI

Linked Data

dbSNP Id: rs903577081
gnomAD v2: 7-37946393-G-A
gnomAD v3: 7-37906791-G-A
gnomAD v4: 7-37906791-G-A
MyVariant Identifiers: chr7:g.37946393G>A (hg19) chr7:g.37906791G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906791G>A , CM000669.2:g.37906791G>A GRCh38
NC_000007.13:g.37946393G>A , CM000669.1:g.37946393G>A GRCh37
NC_000007.12:g.37912918G>A NCBI36
NG_052980.1:g.15133C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*688C>T (SFRP4) MANE Select ENSP00000410715.2:n.*688C>T
ENST00000436072.6:c.*688C>T (SFRP4) ENSP00000410715.2:n.*688C>T
ENST00000476620.1:c.-37-42049G>A (EPDR1) ENSP00000425858.1:n.-37-42049G>A
NM_003014.3:c.*688C>T (SFRP4) NP_003005.2:n.*688C>T
NM_003014.4:c.*688C>T (SFRP4) MANE Select NP_003005.2:n.*688C>T
Search 100 bp 5'
Search 100 bp 3'