Canonical Allele Identifier: CA1864360463
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718579T= , CM000671.2:g.92718579T= GRCh38
NC_000009.11:g.95480861T= , CM000671.1:g.95480861T= GRCh37
NC_000009.10:g.94520682T= NCBI36
NG_033908.1:g.51223A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2066A= MANE Select ENSP00000349351.6:p.Gln689=
ENST00000356884.10:c.2066A= ENSP00000349351.6:p.Gln689=
ENST00000375512.3:c.2066A= ENSP00000364662.3:p.Gln689=
NM_001003800.1:c.2066A= NP_001003800.1:p.Gln689=
NM_015250.3:c.2066A= NP_056065.1:p.Gln689=
XM_017014551.1:c.2147A= XP_016870040.1:p.Gln716=
NM_001003800.2:c.2066A= MANE Select NP_001003800.1:p.Gln689=
NM_015250.4:c.2066A= NP_056065.1:p.Gln689=