Canonical Allele Identifier: CA374036424
Gene: BICD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.95481258A>T (hg19) chr9:g.92718976A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92718976A>T , CM000671.2:g.92718976A>T GRCh38
NC_000009.11:g.95481258A>T , CM000671.1:g.95481258A>T GRCh37
NC_000009.10:g.94521079A>T NCBI36
NG_033908.1:g.50826T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1669T>A MANE Select ENSP00000349351.6:p.Tyr557Asn
ENST00000356884.10:c.1669T>A ENSP00000349351.6:p.Tyr557Asn
ENST00000375512.3:c.1669T>A ENSP00000364662.3:p.Tyr557Asn
NM_001003800.1:c.1669T>A NP_001003800.1:p.Tyr557Asn
NM_015250.3:c.1669T>A NP_056065.1:p.Tyr557Asn
XM_017014551.1:c.1750T>A XP_016870040.1:p.Tyr584Asn
NM_001003800.2:c.1669T>A MANE Select NP_001003800.1:p.Tyr557Asn
NM_015250.4:c.1669T>A NP_056065.1:p.Tyr557Asn
Search 100 bp 5'
Search 100 bp 3'