Canonical Allele Identifier: CA374039416
Gene: BICD2 HGNC NCBI

Linked Data

dbSNP Id: rs1587669291
MyVariant Identifiers: chr9:g.95481683T>G (hg19) chr9:g.92719401T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.92719401T>G , CM000671.2:g.92719401T>G GRCh38
NC_000009.11:g.95481683T>G , CM000671.1:g.95481683T>G GRCh37
NC_000009.10:g.94521504T>G NCBI36
NG_033908.1:g.50401A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356884.11:c.1244A>C MANE Select ENSP00000349351.6:p.Asp415Ala
ENST00000356884.10:c.1244A>C ENSP00000349351.6:p.Asp415Ala
ENST00000375512.3:c.1244A>C ENSP00000364662.3:p.Asp415Ala
NM_001003800.1:c.1244A>C NP_001003800.1:p.Asp415Ala
NM_015250.3:c.1244A>C NP_056065.1:p.Asp415Ala
XM_017014551.1:c.1325A>C XP_016870040.1:p.Asp442Ala
NM_001003800.2:c.1244A>C MANE Select NP_001003800.1:p.Asp415Ala
NM_015250.4:c.1244A>C NP_056065.1:p.Asp415Ala
Search 100 bp 5'
Search 100 bp 3'