Canonical Allele Identifier: CA1864362458
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719471C= , CM000671.2:g.92719471C= GRCh38
NC_000009.11:g.95481753C= , CM000671.1:g.95481753C= GRCh37
NC_000009.10:g.94521574C= NCBI36
NG_033908.1:g.50331G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1174G= MANE Select ENSP00000349351.6:p.Glu392=
ENST00000356884.10:c.1174G= ENSP00000349351.6:p.Glu392=
ENST00000375512.3:c.1174G= ENSP00000364662.3:p.Glu392=
NM_001003800.1:c.1174G= NP_001003800.1:p.Glu392=
NM_015250.3:c.1174G= NP_056065.1:p.Glu392=
XM_017014551.1:c.1255G= XP_016870040.1:p.Glu419=
NM_001003800.2:c.1174G= MANE Select NP_001003800.1:p.Glu392=
NM_015250.4:c.1174G= NP_056065.1:p.Glu392=