Canonical Allele Identifier: CA838194311

Linked Data

dbSNP Id: rs1247035872

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906655A>G , CM000669.2:g.37906655A>G GRCh38
NC_000007.13:g.37946257A>G , CM000669.1:g.37946257A>G GRCh37
NC_000007.12:g.37912782A>G NCBI36
NG_052980.1:g.15269T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*824T>C (SFRP4) MANE Select ENSP00000410715.2:n.*824T>C
ENST00000436072.6:c.*824T>C (SFRP4) ENSP00000410715.2:n.*824T>C
ENST00000476620.1:c.-37-42185A>G (EPDR1) ENSP00000425858.1:n.-37-42185A>G
NM_003014.3:c.*824T>C (SFRP4) NP_003005.2:n.*824T>C
NM_003014.4:c.*824T>C (SFRP4) MANE Select NP_003005.2:n.*824T>C