Canonical Allele Identifier: CA196340082

Gene: BICD2

Linked Data

• ClinVar Variation Id: 952658
• ClinVar RCV Id: RCV001224807 ; RCV003145422
• dbSNP Id: rs369050350
• gnomAD v2: 9-95481122-G-A
• gnomAD v3: 9-92718840-G-A
• gnomAD v4: 9-92718840-G-A
• MyVariant Identifiers: chr9:g.95481122G>A (hg19) ; chr9:g.95481122_95481123delinsAT (hg19) ; chr9:g.92718840G>A (hg38) ; chr9:g.92718840_92718841delinsAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92718840G>A , CM000671.2:g.92718840G>A	GRCh38
NC_000009.11:g.95481122G>A , CM000671.1:g.95481122G>A	GRCh37
NC_000009.10:g.94520943G>A	NCBI36
NG_033908.1:g.50962C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1805C>T MANE Select	ENSP00000349351.6:p.Thr602Met
ENST00000356884.10:c.1805C>T	ENSP00000349351.6:p.Thr602Met
ENST00000375512.3:c.1805C>T	ENSP00000364662.3:p.Thr602Met
NM_001003800.1:c.1805C>T	NP_001003800.1:p.Thr602Met
NM_015250.3:c.1805C>T	NP_056065.1:p.Thr602Met
XM_017014551.1:c.1886C>T	XP_016870040.1:p.Thr629Met
NM_001003800.2:c.1805C>T MANE Select	NP_001003800.1:p.Thr602Met
NM_015250.4:c.1805C>T	NP_056065.1:p.Thr602Met