Canonical Allele Identifier: CA374035741

Gene: BICD2

Linked Data

• gnomAD v4: 9-92718850-C-A
• MyVariant Identifiers: chr9:g.95481132C>A (hg19) ; chr9:g.92718850C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92718850C>A , CM000671.2:g.92718850C>A	GRCh38
NC_000009.11:g.95481132C>A , CM000671.1:g.95481132C>A	GRCh37
NC_000009.10:g.94520953C>A	NCBI36
NG_033908.1:g.50952G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1795G>T MANE Select	ENSP00000349351.6:p.Asp599Tyr
ENST00000356884.10:c.1795G>T	ENSP00000349351.6:p.Asp599Tyr
ENST00000375512.3:c.1795G>T	ENSP00000364662.3:p.Asp599Tyr
NM_001003800.1:c.1795G>T	NP_001003800.1:p.Asp599Tyr
NM_015250.3:c.1795G>T	NP_056065.1:p.Asp599Tyr
XM_017014551.1:c.1876G>T	XP_016870040.1:p.Asp626Tyr
NM_001003800.2:c.1795G>T MANE Select	NP_001003800.1:p.Asp599Tyr
NM_015250.4:c.1795G>T	NP_056065.1:p.Asp599Tyr