Canonical Allele Identifier: CA1864362269
Gene: BICD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719390G= , CM000671.2:g.92719390G= GRCh38
NC_000009.11:g.95481672G= , CM000671.1:g.95481672G= GRCh37
NC_000009.10:g.94521493G= NCBI36
NG_033908.1:g.50412C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1255C= MANE Select ENSP00000349351.6:p.His419=
ENST00000356884.10:c.1255C= ENSP00000349351.6:p.His419=
ENST00000375512.3:c.1255C= ENSP00000364662.3:p.His419=
NM_001003800.1:c.1255C= NP_001003800.1:p.His419=
NM_015250.3:c.1255C= NP_056065.1:p.His419=
XM_017014551.1:c.1336C= XP_016870040.1:p.His446=
NM_001003800.2:c.1255C= MANE Select NP_001003800.1:p.His419=
NM_015250.4:c.1255C= NP_056065.1:p.His419=
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