Canonical Allele Identifier: CA374040231
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95481768C>T (hg19) chr9:g.92719486C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719486C>T , CM000671.2:g.92719486C>T GRCh38
NC_000009.11:g.95481768C>T , CM000671.1:g.95481768C>T GRCh37
NC_000009.10:g.94521589C>T NCBI36
NG_033908.1:g.50316G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1159G>A MANE Select ENSP00000349351.6:p.Val387Met
ENST00000356884.10:c.1159G>A ENSP00000349351.6:p.Val387Met
ENST00000375512.3:c.1159G>A ENSP00000364662.3:p.Val387Met
NM_001003800.1:c.1159G>A NP_001003800.1:p.Val387Met
NM_015250.3:c.1159G>A NP_056065.1:p.Val387Met
XM_017014551.1:c.1240G>A XP_016870040.1:p.Val414Met
NM_001003800.2:c.1159G>A MANE Select NP_001003800.1:p.Val387Met
NM_015250.4:c.1159G>A NP_056065.1:p.Val387Met
Search 100 bp 5'
Search 100 bp 3'