Canonical Allele Identifier: CA5126418
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs747808072
ExAC: 9:95480851 C / A
gnomAD v2: 9-95480851-C-A
gnomAD v4: 9-92718569-C-A
MyVariant Identifiers: chr9:g.95480851C>A (hg19) chr9:g.92718569C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718569C>A , CM000671.2:g.92718569C>A GRCh38
NC_000009.11:g.95480851C>A , CM000671.1:g.95480851C>A GRCh37
NC_000009.10:g.94520672C>A NCBI36
NG_033908.1:g.51233G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2076G>T MANE Select ENSP00000349351.6:p.Thr692=
ENST00000356884.10:c.2076G>T ENSP00000349351.6:p.Thr692=
ENST00000375512.3:c.2076G>T ENSP00000364662.3:p.Thr692=
NM_001003800.1:c.2076G>T NP_001003800.1:p.Thr692=
NM_015250.3:c.2076G>T NP_056065.1:p.Thr692=
XM_017014551.1:c.2157G>T XP_016870040.1:p.Thr719=
NM_001003800.2:c.2076G>T MANE Select NP_001003800.1:p.Thr692=
NM_015250.4:c.2076G>T NP_056065.1:p.Thr692=
Search 100 bp 5'
Search 100 bp 3'