Canonical Allele Identifier: CA1700793210

Linked Data

dbSNP Id: rs762013836

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*687T>A (SFRP4) MANE Select ENSP00000410715.2:n.*687T>A
ENST00000436072.6:c.*687T>A (SFRP4) ENSP00000410715.2:n.*687T>A
ENST00000476620.1:c.-37-42048A>T (EPDR1) ENSP00000425858.1:n.-37-42048A>T
NM_003014.3:c.*687T>A (SFRP4) NP_003005.2:n.*687T>A
NM_003014.4:c.*687T>A (SFRP4) MANE Select NP_003005.2:n.*687T>A