Canonical Allele Identifier: CA374036500
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95481272A>T (hg19) chr9:g.92718990A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718990A>T , CM000671.2:g.92718990A>T GRCh38
NC_000009.11:g.95481272A>T , CM000671.1:g.95481272A>T GRCh37
NC_000009.10:g.94521093A>T NCBI36
NG_033908.1:g.50812T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000356884.11:c.1655T>A MANE Select ENSP00000349351.6:p.Val552Asp
ENST00000356884.10:c.1655T>A ENSP00000349351.6:p.Val552Asp
ENST00000375512.3:c.1655T>A ENSP00000364662.3:p.Val552Asp
NM_001003800.1:c.1655T>A NP_001003800.1:p.Val552Asp
NM_015250.3:c.1655T>A NP_056065.1:p.Val552Asp
XM_017014551.1:c.1736T>A XP_016870040.1:p.Val579Asp
NM_001003800.2:c.1655T>A MANE Select NP_001003800.1:p.Val552Asp
NM_015250.4:c.1655T>A NP_056065.1:p.Val552Asp
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