Canonical Allele Identifier: CA1864361237
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718923G= , CM000671.2:g.92718923G= GRCh38
NC_000009.11:g.95481205G= , CM000671.1:g.95481205G= GRCh37
NC_000009.10:g.94521026G= NCBI36
NG_033908.1:g.50879C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1722C= MANE Select ENSP00000349351.6:p.Ser574=
ENST00000356884.10:c.1722C= ENSP00000349351.6:p.Ser574=
ENST00000375512.3:c.1722C= ENSP00000364662.3:p.Ser574=
NM_001003800.1:c.1722C= NP_001003800.1:p.Ser574=
NM_015250.3:c.1722C= NP_056065.1:p.Ser574=
XM_017014551.1:c.1803C= XP_016870040.1:p.Ser601=
NM_001003800.2:c.1722C= MANE Select NP_001003800.1:p.Ser574=
NM_015250.4:c.1722C= NP_056065.1:p.Ser574=