Canonical Allele Identifier: CA5126518
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1542370
ClinVar RCV Id: RCV002165081 RCV003978518
dbSNP Id: rs35535468
ExAC: 9:95481253 G / T
gnomAD v2: 9-95481253-G-T
gnomAD v3: 9-92718971-G-T
gnomAD v4: 9-92718971-G-T
MyVariant Identifiers: chr9:g.95481253G>T (hg19) chr9:g.92718971G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718971G>T , CM000671.2:g.92718971G>T GRCh38
NC_000009.11:g.95481253G>T , CM000671.1:g.95481253G>T GRCh37
NC_000009.10:g.94521074G>T NCBI36
NG_033908.1:g.50831C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1674C>A MANE Select ENSP00000349351.6:p.Arg558=
ENST00000356884.10:c.1674C>A ENSP00000349351.6:p.Arg558=
ENST00000375512.3:c.1674C>A ENSP00000364662.3:p.Arg558=
NM_001003800.1:c.1674C>A NP_001003800.1:p.Arg558=
NM_015250.3:c.1674C>A NP_056065.1:p.Arg558=
XM_017014551.1:c.1755C>A XP_016870040.1:p.Arg585=
NM_001003800.2:c.1674C>A MANE Select NP_001003800.1:p.Arg558=
NM_015250.4:c.1674C>A NP_056065.1:p.Arg558=
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Search 100 bp 3'