Canonical Allele Identifier: CA374036289
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs1294456292
gnomAD v2: 9-95481227-G-A
gnomAD v4: 9-92718945-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718945G>A , CM000671.2:g.92718945G>A GRCh38
NC_000009.11:g.95481227G>A , CM000671.1:g.95481227G>A GRCh37
NC_000009.10:g.94521048G>A NCBI36
NG_033908.1:g.50857C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1700C>T MANE Select ENSP00000349351.6:p.Thr567Ile
ENST00000356884.10:c.1700C>T ENSP00000349351.6:p.Thr567Ile
ENST00000375512.3:c.1700C>T ENSP00000364662.3:p.Thr567Ile
NM_001003800.1:c.1700C>T NP_001003800.1:p.Thr567Ile
NM_015250.3:c.1700C>T NP_056065.1:p.Thr567Ile
XM_017014551.1:c.1781C>T XP_016870040.1:p.Thr594Ile
NM_001003800.2:c.1700C>T MANE Select NP_001003800.1:p.Thr567Ile
NM_015250.4:c.1700C>T NP_056065.1:p.Thr567Ile