Canonical Allele Identifier: CA196340065
Gene: BICD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1377003
ClinVar RCV Id: RCV001888273
dbSNP Id: rs897077465
gnomAD v4: 9-92718828-C-T
MyVariant Identifiers: chr9:g.95481110C>T (hg19) chr9:g.92718828C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718828C>T , CM000671.2:g.92718828C>T GRCh38
NC_000009.11:g.95481110C>T , CM000671.1:g.95481110C>T GRCh37
NC_000009.10:g.94520931C>T NCBI36
NG_033908.1:g.50974G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1817G>A MANE Select ENSP00000349351.6:p.Ser606Asn
ENST00000356884.10:c.1817G>A ENSP00000349351.6:p.Ser606Asn
ENST00000375512.3:c.1817G>A ENSP00000364662.3:p.Ser606Asn
NM_001003800.1:c.1817G>A NP_001003800.1:p.Ser606Asn
NM_015250.3:c.1817G>A NP_056065.1:p.Ser606Asn
XM_017014551.1:c.1898G>A XP_016870040.1:p.Ser633Asn
NM_001003800.2:c.1817G>A MANE Select NP_001003800.1:p.Ser606Asn
NM_015250.4:c.1817G>A NP_056065.1:p.Ser606Asn
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