Canonical Allele Identifier: CA374036289

Gene: BICD2

Linked Data

• dbSNP Id: rs1294456292
• gnomAD v2: 9-95481227-G-A
• gnomAD v4: 9-92718945-G-A
• MyVariant Identifiers: chr9:g.95481227G>A (hg19) ; chr9:g.92718945G>A (hg38)

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