Canonical Allele Identifier: CA466342737
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95480896G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718614G>C , CM000671.2:g.92718614G>C GRCh38
NC_000009.11:g.95480896G>C , CM000671.1:g.95480896G>C GRCh37
NC_000009.10:g.94520717G>C NCBI36
NG_033908.1:g.51188C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2031C>G MANE Select ENSP00000349351.6:p.Leu677=
ENST00000356884.10:c.2031C>G ENSP00000349351.6:p.Leu677=
ENST00000375512.3:c.2031C>G ENSP00000364662.3:p.Leu677=
NM_001003800.1:c.2031C>G NP_001003800.1:p.Leu677=
NM_015250.3:c.2031C>G NP_056065.1:p.Leu677=
XM_017014551.1:c.2112C>G XP_016870040.1:p.Leu704=
NM_001003800.2:c.2031C>G MANE Select NP_001003800.1:p.Leu677=
NM_015250.4:c.2031C>G NP_056065.1:p.Leu677=
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