Canonical Allele Identifier: CA466029972

Gene: BICD2

Linked Data

• MyVariant Identifiers: chr9:g.95480854G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92718572G>A , CM000671.2:g.92718572G>A	GRCh38
NC_000009.11:g.95480854G>A , CM000671.1:g.95480854G>A	GRCh37
NC_000009.10:g.94520675G>A	NCBI36
NG_033908.1:g.51230C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.2073C>T MANE Select	ENSP00000349351.6:p.Thr691=
ENST00000356884.10:c.2073C>T	ENSP00000349351.6:p.Thr691=
ENST00000375512.3:c.2073C>T	ENSP00000364662.3:p.Thr691=
NM_001003800.1:c.2073C>T	NP_001003800.1:p.Thr691=
NM_015250.3:c.2073C>T	NP_056065.1:p.Thr691=
XM_017014551.1:c.2154C>T	XP_016870040.1:p.Thr718=
NM_001003800.2:c.2073C>T MANE Select	NP_001003800.1:p.Thr691=
NM_015250.4:c.2073C>T	NP_056065.1:p.Thr691=