Canonical Allele Identifier: CA16275467
Gene: POPDC3 HGNC NCBI
BVES-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs11962089

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.105164345A>G , CM000668.2:g.105164345A>G GRCh38
NC_000006.11:g.105612220A>G , CM000668.1:g.105612220A>G GRCh37
NC_000006.10:g.105718913A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000254765.4:c.-251-2185T>C (POPDC3) MANE Select ENSP00000254765.3:n.-251-2185T>C
ENST00000254765.3:c.-251-2185T>C (POPDC3) ENSP00000254765.3:n.-251-2185T>C
ENST00000474760.1:n.164-2185T>C (POPDC3)
NM_022361.4:c.-251-2185T>C (POPDC3) NP_071756.2:n.-251-2185T>C
NR_024539.1:n.64-2185T>C (POPDC3)
NR_037157.1:n.343-2199A>G (BVES-AS1)
XM_011536067.1:c.-251-2185T>C (POPDC3) XP_011534369.1:n.-251-2185T>C
XM_011536068.1:c.-471-582T>C (POPDC3) XP_011534370.1:n.-471-582T>C
XM_011536069.1:c.-352-582T>C (POPDC3) XP_011534371.1:n.-352-582T>C
XM_011536070.1:c.-251-2185T>C (POPDC3) XP_011534372.1:n.-251-2185T>C
XM_011536067.3:c.-251-2185T>C (POPDC3) XP_011534369.1:n.-251-2185T>C
XM_017011194.1:c.-934T>C (POPDC3) XP_016866683.1:n.-934T>C
NM_022361.5:c.-251-2185T>C (POPDC3) MANE Select NP_071756.2:n.-251-2185T>C