Canonical Allele Identifier: CA157145643

Linked Data

dbSNP Id: rs758668767

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906798T>G , CM000669.2:g.37906798T>G GRCh38
NC_000007.13:g.37946400T>G , CM000669.1:g.37946400T>G GRCh37
NC_000007.12:g.37912925T>G NCBI36
NG_052980.1:g.15126A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*681A>C (SFRP4) MANE Select ENSP00000410715.2:n.*681A>C
ENST00000436072.6:c.*681A>C (SFRP4) ENSP00000410715.2:n.*681A>C
ENST00000476620.1:c.-37-42042T>G (EPDR1) ENSP00000425858.1:n.-37-42042T>G
NM_003014.3:c.*681A>C (SFRP4) NP_003005.2:n.*681A>C
NM_003014.4:c.*681A>C (SFRP4) MANE Select NP_003005.2:n.*681A>C