Canonical Allele Identifier: CA1700793177

Linked Data

dbSNP Id: rs1785400855

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906693A>G , CM000669.2:g.37906693A>G GRCh38
NC_000007.13:g.37946295A>G , CM000669.1:g.37946295A>G GRCh37
NC_000007.12:g.37912820A>G NCBI36
NG_052980.1:g.15231T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*786T>C (SFRP4) MANE Select ENSP00000410715.2:n.*786T>C
ENST00000436072.6:c.*786T>C (SFRP4) ENSP00000410715.2:n.*786T>C
ENST00000476620.1:c.-37-42147A>G (EPDR1) ENSP00000425858.1:n.-37-42147A>G
NM_003014.3:c.*786T>C (SFRP4) NP_003005.2:n.*786T>C
NM_003014.4:c.*786T>C (SFRP4) MANE Select NP_003005.2:n.*786T>C