Canonical Allele Identifier: CA5126421
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1785176
ClinVar RCV Id: RCV002421925
dbSNP Id: rs771388324
ExAC: 9:95480868 G / A
gnomAD v2: 9-95480868-G-A
gnomAD v4: 9-92718586-G-A
MyVariant Identifiers: chr9:g.95480868G>A (hg19) chr9:g.92718586G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718586G>A , CM000671.2:g.92718586G>A GRCh38
NC_000009.11:g.95480868G>A , CM000671.1:g.95480868G>A GRCh37
NC_000009.10:g.94520689G>A NCBI36
NG_033908.1:g.51216C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2059C>T MANE Select ENSP00000349351.6:p.Arg687Trp
ENST00000356884.10:c.2059C>T ENSP00000349351.6:p.Arg687Trp
ENST00000375512.3:c.2059C>T ENSP00000364662.3:p.Arg687Trp
NM_001003800.1:c.2059C>T NP_001003800.1:p.Arg687Trp
NM_015250.3:c.2059C>T NP_056065.1:p.Arg687Trp
XM_017014551.1:c.2140C>T XP_016870040.1:p.Arg714Trp
NM_001003800.2:c.2059C>T MANE Select NP_001003800.1:p.Arg687Trp
NM_015250.4:c.2059C>T NP_056065.1:p.Arg687Trp
Search 100 bp 5'
Search 100 bp 3'