Canonical Allele Identifier: CA1864360594
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718641G= , CM000671.2:g.92718641G= GRCh38
NC_000009.11:g.95480923G= , CM000671.1:g.95480923G= GRCh37
NC_000009.10:g.94520744G= NCBI36
NG_033908.1:g.51161C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2004C= MANE Select ENSP00000349351.6:p.Asp668=
ENST00000356884.10:c.2004C= ENSP00000349351.6:p.Asp668=
ENST00000375512.3:c.2004C= ENSP00000364662.3:p.Asp668=
NM_001003800.1:c.2004C= NP_001003800.1:p.Asp668=
NM_015250.3:c.2004C= NP_056065.1:p.Asp668=
XM_017014551.1:c.2085C= XP_016870040.1:p.Asp695=
NM_001003800.2:c.2004C= MANE Select NP_001003800.1:p.Asp668=
NM_015250.4:c.2004C= NP_056065.1:p.Asp668=