Canonical Allele Identifier: CA1864360447

Gene: BICD2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92718569C= , CM000671.2:g.92718569C=	GRCh38
NC_000009.11:g.95480851C= , CM000671.1:g.95480851C=	GRCh37
NC_000009.10:g.94520672C=	NCBI36
NG_033908.1:g.51233G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.2076G= MANE Select	ENSP00000349351.6:p.Thr692=
ENST00000356884.10:c.2076G=	ENSP00000349351.6:p.Thr692=
ENST00000375512.3:c.2076G=	ENSP00000364662.3:p.Thr692=
NM_001003800.1:c.2076G=	NP_001003800.1:p.Thr692=
NM_015250.3:c.2076G=	NP_056065.1:p.Thr692=
XM_017014551.1:c.2157G=	XP_016870040.1:p.Thr719=
NM_001003800.2:c.2076G= MANE Select	NP_001003800.1:p.Thr692=
NM_015250.4:c.2076G=	NP_056065.1:p.Thr692=