Canonical Allele Identifier: CA1864361492
Gene: BICD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719017A= , CM000671.2:g.92719017A= GRCh38
NC_000009.11:g.95481299A= , CM000671.1:g.95481299A= GRCh37
NC_000009.10:g.94521120A= NCBI36
NG_033908.1:g.50785T=

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1628T= MANE Select ENSP00000349351.6:p.Met543=
ENST00000356884.10:c.1628T= ENSP00000349351.6:p.Met543=
ENST00000375512.3:c.1628T= ENSP00000364662.3:p.Met543=
NM_001003800.1:c.1628T= NP_001003800.1:p.Met543=
NM_015250.3:c.1628T= NP_056065.1:p.Met543=
XM_017014551.1:c.1709T= XP_016870040.1:p.Met570=
NM_001003800.2:c.1628T= MANE Select NP_001003800.1:p.Met543=
NM_015250.4:c.1628T= NP_056065.1:p.Met543=