Canonical Allele Identifier: CA16618868
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 422412
ClinVar RCV Id: RCV000479919
dbSNP Id: rs1064795764

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718999G>A , CM000671.2:g.92718999G>A GRCh38
NC_000009.11:g.95481281G>A , CM000671.1:g.95481281G>A GRCh37
NC_000009.10:g.94521102G>A NCBI36
NG_033908.1:g.50803C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1646C>T MANE Select ENSP00000349351.6:p.Pro549Leu
ENST00000356884.10:c.1646C>T ENSP00000349351.6:p.Pro549Leu
ENST00000375512.3:c.1646C>T ENSP00000364662.3:p.Pro549Leu
NM_001003800.1:c.1646C>T NP_001003800.1:p.Pro549Leu
NM_015250.3:c.1646C>T NP_056065.1:p.Pro549Leu
XM_017014551.1:c.1727C>T XP_016870040.1:p.Pro576Leu
NM_001003800.2:c.1646C>T MANE Select NP_001003800.1:p.Pro549Leu
NM_015250.4:c.1646C>T NP_056065.1:p.Pro549Leu