Canonical Allele Identifier: CA374040026
Gene: BICD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719459C>T , CM000671.2:g.92719459C>T GRCh38
NC_000009.11:g.95481741C>T , CM000671.1:g.95481741C>T GRCh37
NC_000009.10:g.94521562C>T NCBI36
NG_033908.1:g.50343G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1186G>A MANE Select ENSP00000349351.6:p.Ala396Thr
ENST00000356884.10:c.1186G>A ENSP00000349351.6:p.Ala396Thr
ENST00000375512.3:c.1186G>A ENSP00000364662.3:p.Ala396Thr
NM_001003800.1:c.1186G>A NP_001003800.1:p.Ala396Thr
NM_015250.3:c.1186G>A NP_056065.1:p.Ala396Thr
XM_017014551.1:c.1267G>A XP_016870040.1:p.Ala423Thr
NM_001003800.2:c.1186G>A MANE Select NP_001003800.1:p.Ala396Thr
NM_015250.4:c.1186G>A NP_056065.1:p.Ala396Thr