Canonical Allele Identifier: CA5126622
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs751407955
ExAC: 9:95481769 C / T
gnomAD v2: 9-95481769-C-T
gnomAD v4: 9-92719487-C-T
MyVariant Identifiers: chr9:g.95481769C>T (hg19) chr9:g.92719487C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719487C>T , CM000671.2:g.92719487C>T GRCh38
NC_000009.11:g.95481769C>T , CM000671.1:g.95481769C>T GRCh37
NC_000009.10:g.94521590C>T NCBI36
NG_033908.1:g.50315G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1158G>A MANE Select ENSP00000349351.6:p.Lys386=
ENST00000356884.10:c.1158G>A ENSP00000349351.6:p.Lys386=
ENST00000375512.3:c.1158G>A ENSP00000364662.3:p.Lys386=
NM_001003800.1:c.1158G>A NP_001003800.1:p.Lys386=
NM_015250.3:c.1158G>A NP_056065.1:p.Lys386=
XM_017014551.1:c.1239G>A XP_016870040.1:p.Lys413=
NM_001003800.2:c.1158G>A MANE Select NP_001003800.1:p.Lys386=
NM_015250.4:c.1158G>A NP_056065.1:p.Lys386=
Search 100 bp 5'
Search 100 bp 3'