Canonical Allele Identifier: CA466342812

Gene: BICD2

Linked Data

• MyVariant Identifiers: chr9:g.95480956G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92718674G>C , CM000671.2:g.92718674G>C	GRCh38
NC_000009.11:g.95480956G>C , CM000671.1:g.95480956G>C	GRCh37
NC_000009.10:g.94520777G>C	NCBI36
NG_033908.1:g.51128C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1971C>G MANE Select	ENSP00000349351.6:p.Ala657=
ENST00000356884.10:c.1971C>G	ENSP00000349351.6:p.Ala657=
ENST00000375512.3:c.1971C>G	ENSP00000364662.3:p.Ala657=
NM_001003800.1:c.1971C>G	NP_001003800.1:p.Ala657=
NM_015250.3:c.1971C>G	NP_056065.1:p.Ala657=
XM_017014551.1:c.2052C>G	XP_016870040.1:p.Ala684=
NM_001003800.2:c.1971C>G MANE Select	NP_001003800.1:p.Ala657=
NM_015250.4:c.1971C>G	NP_056065.1:p.Ala657=