Canonical Allele Identifier: CA1864361255
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718926G= , CM000671.2:g.92718926G= GRCh38
NC_000009.11:g.95481208G= , CM000671.1:g.95481208G= GRCh37
NC_000009.10:g.94521029G= NCBI36
NG_033908.1:g.50876C=

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1719C= MANE Select ENSP00000349351.6:p.Thr573=
ENST00000356884.10:c.1719C= ENSP00000349351.6:p.Thr573=
ENST00000375512.3:c.1719C= ENSP00000364662.3:p.Thr573=
NM_001003800.1:c.1719C= NP_001003800.1:p.Thr573=
NM_015250.3:c.1719C= NP_056065.1:p.Thr573=
XM_017014551.1:c.1800C= XP_016870040.1:p.Thr600=
NM_001003800.2:c.1719C= MANE Select NP_001003800.1:p.Thr573=
NM_015250.4:c.1719C= NP_056065.1:p.Thr573=