Canonical Allele Identifier: CA196340502

Gene: BICD2

Linked Data

• ClinVar Variation Id: 2961065
• ClinVar RCV Id: RCV003819776
• dbSNP Id: rs1048333844
• MyVariant Identifiers: chr9:g.95481310G>A (hg19) ; chr9:g.92719028G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92719028G>A , CM000671.2:g.92719028G>A	GRCh38
NC_000009.11:g.95481310G>A , CM000671.1:g.95481310G>A	GRCh37
NC_000009.10:g.94521131G>A	NCBI36
NG_033908.1:g.50774C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1617C>T MANE Select	ENSP00000349351.6:p.His539=
ENST00000356884.10:c.1617C>T	ENSP00000349351.6:p.His539=
ENST00000375512.3:c.1617C>T	ENSP00000364662.3:p.His539=
NM_001003800.1:c.1617C>T	NP_001003800.1:p.His539=
NM_015250.3:c.1617C>T	NP_056065.1:p.His539=
XM_017014551.1:c.1698C>T	XP_016870040.1:p.His566=
NM_001003800.2:c.1617C>T MANE Select	NP_001003800.1:p.His539=
NM_015250.4:c.1617C>T	NP_056065.1:p.His539=