Canonical Allele Identifier: CA374034390
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs1173011262
gnomAD v4: 9-92718635-T-G
MyVariant Identifiers: chr9:g.95480917T>G (hg19) chr9:g.92718635T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718635T>G , CM000671.2:g.92718635T>G GRCh38
NC_000009.11:g.95480917T>G , CM000671.1:g.95480917T>G GRCh37
NC_000009.10:g.94520738T>G NCBI36
NG_033908.1:g.51167A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2010A>C MANE Select ENSP00000349351.6:p.Glu670Asp
ENST00000356884.10:c.2010A>C ENSP00000349351.6:p.Glu670Asp
ENST00000375512.3:c.2010A>C ENSP00000364662.3:p.Glu670Asp
NM_001003800.1:c.2010A>C NP_001003800.1:p.Glu670Asp
NM_015250.3:c.2010A>C NP_056065.1:p.Glu670Asp
XM_017014551.1:c.2091A>C XP_016870040.1:p.Glu697Asp
NM_001003800.2:c.2010A>C MANE Select NP_001003800.1:p.Glu670Asp
NM_015250.4:c.2010A>C NP_056065.1:p.Glu670Asp
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