Canonical Allele Identifier: CA466342757
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95480914C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718632C>G , CM000671.2:g.92718632C>G GRCh38
NC_000009.11:g.95480914C>G , CM000671.1:g.95480914C>G GRCh37
NC_000009.10:g.94520735C>G NCBI36
NG_033908.1:g.51170G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2013G>C MANE Select ENSP00000349351.6:p.Ala671=
ENST00000356884.10:c.2013G>C ENSP00000349351.6:p.Ala671=
ENST00000375512.3:c.2013G>C ENSP00000364662.3:p.Ala671=
NM_001003800.1:c.2013G>C NP_001003800.1:p.Ala671=
NM_015250.3:c.2013G>C NP_056065.1:p.Ala671=
XM_017014551.1:c.2094G>C XP_016870040.1:p.Ala698=
NM_001003800.2:c.2013G>C MANE Select NP_001003800.1:p.Ala671=
NM_015250.4:c.2013G>C NP_056065.1:p.Ala671=
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