Canonical Allele Identifier: CA466342989

Gene: BICD2

Linked Data

• MyVariant Identifiers: chr9:g.95481169T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92718887T>G , CM000671.2:g.92718887T>G	GRCh38
NC_000009.11:g.95481169T>G , CM000671.1:g.95481169T>G	GRCh37
NC_000009.10:g.94520990T>G	NCBI36
NG_033908.1:g.50915A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1758A>C MANE Select	ENSP00000349351.6:p.Leu586=
ENST00000356884.10:c.1758A>C	ENSP00000349351.6:p.Leu586=
ENST00000375512.3:c.1758A>C	ENSP00000364662.3:p.Leu586=
NM_001003800.1:c.1758A>C	NP_001003800.1:p.Leu586=
NM_015250.3:c.1758A>C	NP_056065.1:p.Leu586=
XM_017014551.1:c.1839A>C	XP_016870040.1:p.Leu613=
NM_001003800.2:c.1758A>C MANE Select	NP_001003800.1:p.Leu586=
NM_015250.4:c.1758A>C	NP_056065.1:p.Leu586=