Canonical Allele Identifier: CA5126502
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1102972
ClinVar RCV Id: RCV001426459
dbSNP Id: rs375060340
gnomAD v2: 9-95481211-G-T
gnomAD v3: 9-92718929-G-T
gnomAD v4: 9-92718929-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718929G>T , CM000671.2:g.92718929G>T GRCh38
NC_000009.11:g.95481211G>T , CM000671.1:g.95481211G>T GRCh37
NC_000009.10:g.94521032G>T NCBI36
NG_033908.1:g.50873C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1716C>A MANE Select ENSP00000349351.6:p.Arg572=
ENST00000356884.10:c.1716C>A ENSP00000349351.6:p.Arg572=
ENST00000375512.3:c.1716C>A ENSP00000364662.3:p.Arg572=
NM_001003800.1:c.1716C>A NP_001003800.1:p.Arg572=
NM_015250.3:c.1716C>A NP_056065.1:p.Arg572=
XM_017014551.1:c.1797C>A XP_016870040.1:p.Arg599=
NM_001003800.2:c.1716C>A MANE Select NP_001003800.1:p.Arg572=
NM_015250.4:c.1716C>A NP_056065.1:p.Arg572=