Canonical Allele Identifier: CA466029953

Gene: BICD2

Linked Data

• MyVariant Identifiers: chr9:g.95480830G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92718548G>T , CM000671.2:g.92718548G>T	GRCh38
NC_000009.11:g.95480830G>T , CM000671.1:g.95480830G>T	GRCh37
NC_000009.10:g.94520651G>T	NCBI36
NG_033908.1:g.51254C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.2097C>A MANE Select	ENSP00000349351.6:p.Ala699=
ENST00000356884.10:c.2097C>A	ENSP00000349351.6:p.Ala699=
ENST00000375512.3:c.2097C>A	ENSP00000364662.3:p.Ala699=
NM_001003800.1:c.2097C>A	NP_001003800.1:p.Ala699=
NM_015250.3:c.2097C>A	NP_056065.1:p.Ala699=
XM_017014551.1:c.2178C>A	XP_016870040.1:p.Ala726=
NM_001003800.2:c.2097C>A MANE Select	NP_001003800.1:p.Ala699=
NM_015250.4:c.2097C>A	NP_056065.1:p.Ala699=