Canonical Allele Identifier: CA466342733

Gene: BICD2

Linked Data

• dbSNP Id: rs1221820883
• gnomAD v4: 9-92719097-T-G
• MyVariant Identifiers: chr9:g.95481379T>G (hg19) ; chr9:g.92719097T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.92719097T>G , CM000671.2:g.92719097T>G	GRCh38
NC_000009.11:g.95481379T>G , CM000671.1:g.95481379T>G	GRCh37
NC_000009.10:g.94521200T>G	NCBI36
NG_033908.1:g.50705A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356884.11:c.1548A>C MANE Select	ENSP00000349351.6:p.Thr516=
ENST00000356884.10:c.1548A>C	ENSP00000349351.6:p.Thr516=
ENST00000375512.3:c.1548A>C	ENSP00000364662.3:p.Thr516=
NM_001003800.1:c.1548A>C	NP_001003800.1:p.Thr516=
NM_015250.3:c.1548A>C	NP_056065.1:p.Thr516=
XM_017014551.1:c.1629A>C	XP_016870040.1:p.Thr543=
NM_001003800.2:c.1548A>C MANE Select	NP_001003800.1:p.Thr516=
NM_015250.4:c.1548A>C	NP_056065.1:p.Thr516=