Canonical Allele Identifier: CA374040229
Gene: BICD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719485A>T , CM000671.2:g.92719485A>T GRCh38
NC_000009.11:g.95481767A>T , CM000671.1:g.95481767A>T GRCh37
NC_000009.10:g.94521588A>T NCBI36
NG_033908.1:g.50317T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1160T>A MANE Select ENSP00000349351.6:p.Val387Glu
ENST00000356884.10:c.1160T>A ENSP00000349351.6:p.Val387Glu
ENST00000375512.3:c.1160T>A ENSP00000364662.3:p.Val387Glu
NM_001003800.1:c.1160T>A NP_001003800.1:p.Val387Glu
NM_015250.3:c.1160T>A NP_056065.1:p.Val387Glu
XM_017014551.1:c.1241T>A XP_016870040.1:p.Val414Glu
NM_001003800.2:c.1160T>A MANE Select NP_001003800.1:p.Val387Glu
NM_015250.4:c.1160T>A NP_056065.1:p.Val387Glu