Canonical Allele Identifier: CA2682437840

Linked Data

gnomAD v4: 7-37906658-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37906658T>C , CM000669.2:g.37906658T>C GRCh38
NC_000007.13:g.37946260T>C , CM000669.1:g.37946260T>C GRCh37
NC_000007.12:g.37912785T>C NCBI36
NG_052980.1:g.15266A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000436072.7:c.*821A>G (SFRP4) MANE Select ENSP00000410715.2:n.*821A>G
ENST00000436072.6:c.*821A>G (SFRP4) ENSP00000410715.2:n.*821A>G
ENST00000476620.1:c.-37-42182T>C (EPDR1) ENSP00000425858.1:n.-37-42182T>C
NM_003014.3:c.*821A>G (SFRP4) NP_003005.2:n.*821A>G
NM_003014.4:c.*821A>G (SFRP4) MANE Select NP_003005.2:n.*821A>G