Canonical Allele Identifier: CA573962498
Gene: SFRP4 HGNC NCBI
EPDR1 HGNC NCBI

Linked Data

dbSNP Id: rs1387786656
gnomAD v2: 7-37946310-T-C
MyVariant Identifiers: chr7:g.37946310T>C (hg19) chr7:g.37906708T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906708T>C , CM000669.2:g.37906708T>C GRCh38
NC_000007.13:g.37946310T>C , CM000669.1:g.37946310T>C GRCh37
NC_000007.12:g.37912835T>C NCBI36
NG_052980.1:g.15216A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*771A>G (SFRP4) MANE Select ENSP00000410715.2:n.*771A>G
ENST00000436072.6:c.*771A>G (SFRP4) ENSP00000410715.2:n.*771A>G
ENST00000476620.1:c.-37-42132T>C (EPDR1) ENSP00000425858.1:n.-37-42132T>C
NM_003014.3:c.*771A>G (SFRP4) NP_003005.2:n.*771A>G
NM_003014.4:c.*771A>G (SFRP4) MANE Select NP_003005.2:n.*771A>G
Search 100 bp 5'
Search 100 bp 3'