Canonical Allele Identifier: CA466342817
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95480959A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718677A>T , CM000671.2:g.92718677A>T GRCh38
NC_000009.11:g.95480959A>T , CM000671.1:g.95480959A>T GRCh37
NC_000009.10:g.94520780A>T NCBI36
NG_033908.1:g.51125T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1968T>A MANE Select ENSP00000349351.6:p.Ile656=
ENST00000356884.10:c.1968T>A ENSP00000349351.6:p.Ile656=
ENST00000375512.3:c.1968T>A ENSP00000364662.3:p.Ile656=
NM_001003800.1:c.1968T>A NP_001003800.1:p.Ile656=
NM_015250.3:c.1968T>A NP_056065.1:p.Ile656=
XM_017014551.1:c.2049T>A XP_016870040.1:p.Ile683=
NM_001003800.2:c.1968T>A MANE Select NP_001003800.1:p.Ile656=
NM_015250.4:c.1968T>A NP_056065.1:p.Ile656=
Search 100 bp 5'
Search 100 bp 3'