Canonical Allele Identifier: CA1700793215

Linked Data

dbSNP Id: rs1785402129

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906796T>G , CM000669.2:g.37906796T>G GRCh38
NC_000007.13:g.37946398T>G , CM000669.1:g.37946398T>G GRCh37
NC_000007.12:g.37912923T>G NCBI36
NG_052980.1:g.15128A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*683A>C (SFRP4) MANE Select ENSP00000410715.2:n.*683A>C
ENST00000436072.6:c.*683A>C (SFRP4) ENSP00000410715.2:n.*683A>C
ENST00000476620.1:c.-37-42044T>G (EPDR1) ENSP00000425858.1:n.-37-42044T>G
NM_003014.3:c.*683A>C (SFRP4) NP_003005.2:n.*683A>C
NM_003014.4:c.*683A>C (SFRP4) MANE Select NP_003005.2:n.*683A>C