Canonical Allele Identifier: CA374034037
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95480873G>T (hg19) chr9:g.92718591G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718591G>T , CM000671.2:g.92718591G>T GRCh38
NC_000009.11:g.95480873G>T , CM000671.1:g.95480873G>T GRCh37
NC_000009.10:g.94520694G>T NCBI36
NG_033908.1:g.51211C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.2054C>A MANE Select ENSP00000349351.6:p.Thr685Asn
ENST00000356884.10:c.2054C>A ENSP00000349351.6:p.Thr685Asn
ENST00000375512.3:c.2054C>A ENSP00000364662.3:p.Thr685Asn
NM_001003800.1:c.2054C>A NP_001003800.1:p.Thr685Asn
NM_015250.3:c.2054C>A NP_056065.1:p.Thr685Asn
XM_017014551.1:c.2135C>A XP_016870040.1:p.Thr712Asn
NM_001003800.2:c.2054C>A MANE Select NP_001003800.1:p.Thr685Asn
NM_015250.4:c.2054C>A NP_056065.1:p.Thr685Asn
Search 100 bp 5'
Search 100 bp 3'