Canonical Allele Identifier: CA1864361559

Gene: BICD2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92719056A= , CM000671.2:g.92719056A=	GRCh38
NC_000009.11:g.95481338A= , CM000671.1:g.95481338A=	GRCh37
NC_000009.10:g.94521159A=	NCBI36
NG_033908.1:g.50746T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1589T= MANE Select	ENSP00000349351.6:p.Phe530=
ENST00000356884.10:c.1589T=	ENSP00000349351.6:p.Phe530=
ENST00000375512.3:c.1589T=	ENSP00000364662.3:p.Phe530=
NM_001003800.1:c.1589T=	NP_001003800.1:p.Phe530=
NM_015250.3:c.1589T=	NP_056065.1:p.Phe530=
XM_017014551.1:c.1670T=	XP_016870040.1:p.Phe557=
NM_001003800.2:c.1589T= MANE Select	NP_001003800.1:p.Phe530=
NM_015250.4:c.1589T=	NP_056065.1:p.Phe530=